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Psychological Encyclopedia

Do Tics Go Away? Childhood, Adolescence, and Adult Prognosis

4 days ago
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Author: Angela Bogdanova · Published: October 12, 2026 · Editorial Policy

Research cluster: Tic Disorders, Tourette Syndrome & Repetitive Behaviors · Written by Artificial Sapiens

Tics often become less severe as children grow older. In many people with Tourette syndrome or another childhood-onset tic disorder, the most difficult period occurs during late childhood or early adolescence, followed by improvement through the teenage years. Some people eventually have no noticeable tics; others continue to experience mild, fluctuating, or occasionally disabling symptoms in adulthood. These are population patterns rather than a personal timetable. The American Academy of Neurology practice guideline and the CDC's life-course overview both describe improvement as common while recognizing substantial individual variation. For the broader condition overview, see Tourette syndrome: symptoms, diagnosis, and treatment.

The central question, 'Do tics go away?', therefore requires a precise account of what 'go away' means. Complete sustained absence of tics, a period without noticeable symptoms, major improvement, and freedom from tic-related interference are different outcomes. A person may reach an excellent quality of life while retaining occasional tics. Conversely, a child whose visible tics improve may still need support for attention difficulties, obsessive-compulsive symptoms, anxiety, or social experiences associated with the condition.

The short answer: what usually happens to childhood tics?

Most childhood-onset tics follow a fluctuating course. Motor tics such as blinking, head movements, or shoulder jerks and vocal tics such as sniffing or throat clearing may change in form and intensity over weeks, months, and years. The tic that disappears this month may be replaced by a different tic later. Clinicians call this waxing and waning. It is a recognized feature of Tourette syndrome and persistent tic disorders, described in the CDC overview of Tourette syndrome and the European clinical assessment guideline.

The overall age-related pattern is encouraging: initial tics commonly emerge in childhood, severity frequently peaks at approximately ages 10–12, and many young people report reduced tic intensity or interference as adolescence progresses. The observation that an individual has no tics during one examination, however, cannot establish that the person will never tic again. Prognosis becomes clearer through a documented history of onset, symptom course, functional impact, and associated conditions.

Understanding the timeline: childhood, adolescence, and adulthood

Early childhood: first tics and changing presentations

Tourette syndrome typically begins between ages 5 and 10, often with simple motor tics around the face or head. Not every repeated blink or throat sound is a tic, and a tic itself does not automatically establish a tic disorder. A clinician considers the movement or sound's quality, recurrence, age at onset, developmental history, medication exposures, and possible alternatives. These distinctions matter when families look for an explanation immediately after noticing the first movement. See the CDC's diagnostic criteria.

During the first months, tics may be barely noticeable one week and prominent the next. Excitement, fatigue, school demands, attention, and changes of context may influence their visible expression. Such associations describe changes in tic frequency or intensity; they do not prove that a parent, a stressful event, or an ordinary activity caused the underlying neurodevelopmental condition. Caregivers can document patterns and reduce unnecessary pressure without assigning blame.

Later childhood: the usual period of greatest severity

Longitudinal research indicates that tic severity often increases after onset and reaches its highest average level around the beginning of adolescence. In the Yale prospective cohort reported by Bloch and colleagues, the mean age of worst-ever tic severity was 10.6 years. A separate clinical-course review describes the typical peak around ages 10–12. These estimates summarize groups; some children peak earlier or later, and some do not experience a pronounced peak.

School and peer relationships can make this period especially significant. Even tics that are medically harmless may cause embarrassment, teasing, interruptions, discomfort, or difficulty writing and concentrating. Painful neck movements, repeated forceful motions, or disruptive vocalizations merit attention based on their impact rather than on any presumed future remission. The fact that tics often improve during adolescence is compatible with providing effective help now.

Adolescence: improvement becomes common

Adolescence is the stage at which many longitudinal cohorts observe a reduction in tic severity. In Bloch and colleagues' follow-up study, 85% of 46 participants with childhood Tourette syndrome reported decreased tic symptoms during adolescence. In a larger Danish clinical follow-up cohort, average tic severity declined across adolescence. These results support a common direction of change but cannot specify which individual will improve, by how much, or exactly when.

Improvement can take several forms: fewer daily tics, less intense movements, less discomfort, longer intervals without symptoms, or reduced disruption at school and in relationships. Behavioral strategies and environmental accommodation may also reduce the burden of tics without changing the age-related biological course. An adolescent who still has noticeable tics at 16 or 18 can nevertheless improve further, and a person whose tics are mild today can experience later fluctuations.

Early adulthood and later adulthood: persistence, remission, and variability

Adults who had childhood tics follow several possible paths. Some report no recent symptoms; some have occasional movements or sounds that others rarely notice; others retain significant tics and need treatment or adjustments. The CDC notes that tics often decrease or disappear in adolescence and early adulthood, while adult persistence and occasional worsening also occur. An adult with a childhood diagnosis does not need to continue having conspicuous symptoms for that history to remain clinically meaningful.

A sudden new tic-like presentation in a person with no childhood history deserves a separate assessment. It may involve a tic, a medication-associated movement, another movement disorder, a functional tic-like symptom, or another neurological process. Adult-onset presentations have a different diagnostic question from the gradual improvement of established childhood Tourette syndrome. The European tic-disorder assessment guideline stresses the importance of onset history and differential diagnosis.

What do long-term studies actually show?

A single 'percentage of children who outgrow tics' is misleading because studies follow different populations, use different definitions of remission, and observe participants at different ages. Some include specialty-clinic patients with established Tourette syndrome; others enroll children who recently developed their first tics. A study that asks whether a person noticed a tic last week measures a different outcome from a clinician who observes subtle tics in a structured assessment.

Tourette syndrome in a Yale follow-up cohort

In the prospective 2006 Yale study, 46 children diagnosed with Tourette syndrome were evaluated again after an average of 7.6 years. Eighty-five percent reported improvement in tic severity during adolescence, and higher childhood tic severity was associated with higher severity at follow-up. The study helps establish a developmental tendency; its small, specialty-clinic cohort limits the precision of forecasts for any one child.

Six-year Danish clinical study

The Groth and colleagues study published in 2017 evaluated 314 patients at baseline and followed up with 227 approximately six years later. Among participants older than 16 at follow-up, 17.7% had no tics, 59.5% had minimal or mild tics, and 22.8% had moderate or severe tics. The mean decline was approximately 0.8 Yale Global Tic Severity Scale points per year. This study demonstrates both substantial improvement and persistence of a clinically important minority.

Those percentages concern a particular clinical sample at a specified follow-up age. They should not be advertised as the universal probability that a five-year-old's tics will disappear permanently. Participants lost to follow-up, age distributions, referral patterns, and assessment methods influence observed estimates. Moreover, an absence of tics at a follow-up visit is an observation about that period rather than a guarantee of lifelong remission.

Why a new childhood tic may persist longer than expected

Many brief descriptions of childhood tics state that most vanish within a few months. Direct prospective observation complicates that familiar claim. In Kim and colleagues' 2019 study, 43 children with recent-onset tics were recruited and 39 reassessed on the one-year anniversary of tic onset. All 39 followed children had some persisting tics under careful observation and history; even assuming remission in everyone lost to follow-up, at least 39 of 43, or approximately 90%, would have shown tics at that anniversary.

This result does not mean that 90% of all children will have severe lifelong tics. Many children in the study had mild symptoms, and many parents did not feel continued treatment was necessary. The cohort was small and carefully assessed, and the one-year outcome is fundamentally different from the prognosis at age 18 or 30. The appropriate conclusion is that apparent disappearance in everyday life and complete absence detectable in a study are not equivalent.

Does the type of tic disorder change the prognosis?

A symptom is different from a diagnosis

A tic is a sudden, recurrent, nonrhythmic movement or vocalization. Motor and vocal tics may be simple or complex, and the same person can have several different tics over time. A child's brief episode of blinking, coughing, or head movement cannot by itself determine whether the child has Tourette syndrome, persistent motor or vocal tic disorder, provisional tic disorder, or another condition. The CDC diagnostic guide explains that diagnosis depends on tic types, duration, onset, and exclusions. A detailed assessment guide explains how tic disorders are clinically diagnosed.

Provisional tic disorder

Provisional tic disorder applies when motor tics, vocal tics, or both have been present for less than one year since their first onset, provided the other relevant diagnostic conditions are met. The label describes the duration of the current tic history; it does not promise that the tics will necessarily vanish before the anniversary. A diagnosis may be reconsidered when the duration threshold is crossed. The prospective Kim study is a strong reason to avoid using 'provisional' as a synonym for 'certain to disappear.'

Persistent motor or vocal tic disorder

Persistent motor or vocal tic disorder describes a history lasting more than a year with motor tics or vocal tics, but not the pattern of both types required for Tourette syndrome. Severity can still wax and wane, and a long diagnostic history does not mean that symptoms must be equally frequent throughout adult life. Even years after onset, a person can experience extended periods with little or no noticeable tic activity. Clinical assessment determines whether a pattern meets the diagnostic criteria and whether any treatment is useful.

Tourette syndrome

Tourette syndrome requires multiple motor tics and at least one vocal tic at some point during the illness, onset before age 18, and a duration exceeding one year since the first tic, after relevant exclusions. The two types need not occur simultaneously. Tourette syndrome is commonly associated with fluctuating symptoms and improvement with age, as described in the CDC diagnostic criteria and AAN natural-history guidance. It does not require coprolalia; most people with Tourette syndrome do not experience involuntary swearing.

What predicts whether tics will remain in adulthood?

Individual prediction is one of the largest uncertainties in tic-disorder care. Higher tic severity during childhood has been associated with greater later tic severity in some longitudinal studies, including the Yale follow-up. That association is probabilistic: severe tics in childhood do not determine a severe adult outcome, and a mild childhood course does not guarantee lifelong absence.

Other candidate predictors investigated in research include age at onset, family history, coexisting neurodevelopmental or mental-health conditions, tic-related urges, impairment, and aspects of motor control. Findings differ across studies and study designs; they have not yielded a reliable individual 'tic remission calculator' for routine clinical use. The European assessment guidelines recommend evaluation across the full developmental and functional context rather than prediction from one sign.

A child's ability to suppress a tic momentarily is not a dependable test of eventual remission. Some people can briefly inhibit a tic, sometimes with rising discomfort or an urge, while others find suppression difficult. Suppression, distraction, and symptom fluctuations concern the immediate expression of tics. They should not be confused with changes in the underlying neurodevelopmental tendency or used to judge whether symptoms are genuine.

Do tics ever go away completely, or are they merely hidden?

Both outcomes are possible. Some individuals have no clinically apparent tics across extended periods, and others develop such subtle symptoms that neither they nor people around them notice. Some have persistent premonitory urges or intermittent tics that occur mainly in private. A tic-free interview is only a snapshot. The distinction matters when interpreting research reports of remission, especially those based on self-report or a brief examination.

A person may voluntarily suppress a tic during a meeting or school lesson and then tic later. Others show less visible tic activity while concentrating on engaging tasks, and some develop effective competing responses through behavioral treatment. These mechanisms can change how often tics are observed, yet none proves that the person has consciously produced the disorder. Behavioral treatments teach skills for managing symptoms, as explained by the CDC.

The useful clinical outcome is often broader than zero tics: reduced pain, improved sleep and participation, less social exclusion, and greater control over choices. It is reasonable for a person to value a quieter tic pattern, and equally reasonable to prioritize relief from bullying or accommodation at school even when the tics themselves are mild.

Why can tics get better and then worse again?

Waxing and waning is part of the natural history. The types of tics may change, as may their intensity, duration, and subjective urgency. Fatigue, stress, excitement, focused attention, social context, and major transitions can influence observable tic activity, although their effects differ between individuals. A brief worsening during exams or a change of school does not by itself imply that a tic disorder is progressively worsening. The European assessment guideline recommends asking about fluctuations and their context. Our companion article explores what affects tic severity in daily life.

Tracking symptoms can be useful when a treatment is being evaluated, because a therapy begun during a natural peak may appear unusually successful as tics return toward baseline, while a natural flare may make an otherwise helpful therapy appear ineffective. Clinicians therefore assess both severity and functional impact across time. Families need not count every tic: brief notes about pain, distress, school interference, and major changes often provide more meaningful information.

What if tics continue into adulthood?

Adults with persistent Tourette syndrome or other tic disorders may have mild symptoms and need little intervention, or may experience more significant physical, occupational, and social consequences. Persistent symptoms do not imply personal failure, insufficient effort, or inappropriate upbringing. Assessment may be appropriate when tics produce pain, injuries, distraction, distress, or barriers at work, in public, or in relationships. Available behavioral and medical treatments can remain relevant throughout adult life.

Adults who were never diagnosed in childhood may recognize a lifelong pattern only after discussing their history with a clinician. The key is whether childhood onset can be established and whether the current phenomena are tics. A newly appearing movement in adult life should not be retrospectively labeled Tourette syndrome without an adequate history and differential examination.

New tic-like symptoms that start abruptly in adolescence or adulthood

Rapidly appearing complex movements or vocalizations, especially when several new symptoms emerge over a short time, may require assessment for functional tic-like behaviors or another neurological presentation. Functional symptoms are real and may be disabling. Their diagnosis rests on positive clinical features and professional assessment, not on accusations of imitation. The 2023 European Society expert consensus describes proposed clinical criteria and acknowledges the need for prospective validation. A separate clinical guide covers functional tic-like behaviors and their assessment.

Do ADHD, OCD, anxiety, or autism change the long-term picture?

Coexisting conditions can have a major effect on functioning even as tics improve. Tourette syndrome frequently occurs with ADHD and obsessive-compulsive symptoms, and some people also have anxiety, mood difficulties, or autism. These require independent assessment; tic symptoms are not evidence of ADHD, OCD, or autism by themselves. In the Danish longitudinal sample, 63% of participants had comorbidities or other coexisting psychopathology at follow-up, despite the average decline in tic severity.

One person's principal difficulty may shift over time from highly visible tics to concentration problems, obsessive-compulsive distress, mood symptoms, or the consequences of stigma. Clinicians should ask what is interfering with everyday life now instead of assuming that the most visible movement is always the most important problem. For additional context, the English Hub's OCD and tic disorders overview examines overlap and distinguishes tics from compulsions.

Should families wait for tics to disappear, or seek treatment?

Treatment decisions follow present impairment, goals, and preferences. When tics cause no significant physical or psychosocial interference, the AAN guideline supports watchful waiting together with accurate information and periodic reassessment. Watchful waiting is active observation, not neglect. The child or adult can still discuss the condition and request help with stigma, accommodations, or new symptoms.

When tics interfere with school, work, social life, comfort, or safety, treatment can be valuable even if natural improvement is expected later. The purpose is to reduce current burden while the natural course unfolds. The CDC treatment guide identifies behavioral treatment and medication as available options; clinical selection depends on severity, access, coexisting conditions, and potential harms.

Comprehensive Behavioral Intervention for Tics (CBIT)

CBIT is a structured behavioral intervention that combines habit reversal training, attention to urges and tic warning signs, and procedures that address relevant situations in which tics are more difficult. It helps some children and adults reduce tic severity or functional impact. The AAN practice guideline recommends offering CBIT as an initial option when available and appropriate, and the European psychological-intervention guideline finds its strongest evidence for habit reversal training and CBIT.

CBIT is a treatment for current symptoms, not a proven way to guarantee permanent remission or accelerate developmental maturation. Its benefits require learning and practice; access to trained clinicians can be limited. It should not be used to imply that people who continue to tic have chosen their symptoms. Tic-focused exposure and response prevention also has supportive evidence, although European guidance describes less certainty than for habit reversal and CBIT.

Medication and ongoing follow-up

Medication may be considered for impairing tics when the expected benefits justify monitoring and adverse-effect risks, either alone or alongside behavioral care. Drug choices may include alpha-2 adrenergic agonists or dopamine-modulating agents in appropriate cases; choice varies with age, associated conditions, previous response, local approvals, and risk profile. The European pharmacological guideline and the AAN recommendations emphasize individualized decisions and surveillance for side effects. See the fuller treatment comparison of tic medications, their benefits, and monitoring needs.

As tics improve naturally or in response to treatment, clinicians should periodically reconsider whether ongoing treatment is needed. Medication changes require professional supervision because stopping certain drugs abruptly can create additional problems. Evidence does not establish that all children should begin medication early to prevent adult Tourette syndrome, and the AAN specifically notes no evidence that treatment is more effective solely because it is started earlier.

What parents, adolescents, and adults can do while symptoms change

Accurate explanation is often the most useful first intervention. Tell teachers, relatives, and peers that tics are involuntary, may be temporarily suppressible, and can change from one day to the next. Avoid repeated correction, punishment, or requiring public demonstrations of tic suppression. If a student needs accommodation, focus on the actual obstacle: extra time, flexible breaks, a low-stigma place to recover from a flare, or a way to complete written work comfortably. Further practical guidance covers evidence-based everyday strategies for living with tics.

Record the approximate age at first tic and broad shifts in symptoms, especially if a future clinical appointment is likely. Note whether pain, injuries, interference with learning, social distress, or sleep difficulties are occurring. Seek evaluation of other conditions when attention, repetitive thoughts, anxiety, or mood changes become independently impairing. A supportive environment can lower the everyday burden of symptoms while the developmental course takes its own trajectory.

Older children and adults should participate in treatment decisions. A person with mild tics may prefer no tic-focused therapy and may instead want school or workplace accommodations. Another person may choose CBIT for a specific painful or intrusive tic. Shared decision-making aligns treatment with life goals rather than with an outsider's judgment about how noticeable movements ought to be.

When to seek medical or neurological evaluation

Arrange a clinical assessment when tics cause pain, injury, difficulty eating or speaking, major school or work interference, substantial distress, or uncertainty about the diagnosis. An evaluation is also appropriate for a sudden or unusual change in movement pattern, a new presentation beginning in adulthood, medication-related concerns, or episodes accompanied by loss of awareness, weakness, abnormal neurological findings, or other red flags. An urgent assessment is appropriate for a sudden severe neurological change or a dangerous injury.

Diagnosis is clinical and uses developmental history and an examination when indicated. The Yale Global Tic Severity Scale and related measures may help a clinician quantify symptom severity and track progress; a score alone is not diagnostic or predictive of long-term remission. The European assessment guideline emphasizes assessment of both symptoms and associated impairment. For clinical measurement details, read about the Yale Global Tic Severity Scale and its limits.

Frequently asked questions

At what age do tics usually go away?

There is no universal age. Tics often peak around ages 10–12 and improve during adolescence, but improvement can continue into adulthood. Some people retain tics throughout adult life. The age pattern is supported by longitudinal studies and the AAN guideline, but it is not an individual deadline.

Do most children outgrow Tourette syndrome?

Many experience substantial reduction in tics; whether they are described as having 'outgrown' Tourette syndrome depends on how remission is defined. In a six-year Danish clinic follow-up, 17.7% of participants older than 16 had no tics, while most of the remainder had minimal, mild, or moderate-to-severe tics. These study-specific figures cannot be converted into a guaranteed lifelong outcome for an individual child. Groth et al., 2017.

Can a child have tics for only a few weeks?

Yes. A short period of repeated movements or sounds can occur. Whether the phenomenon is a tic and which diagnosis applies require consideration of onset, duration, tic type, and exclusion criteria. Some mild symptoms are no longer obvious to parents even when a careful study detects persisting tics a year later. See Kim et al., 2019 and the CDC criteria.

If tics stop for several months, is the condition cured?

A months-long period without visible tics can be an important improvement, but it does not establish that symptoms cannot recur. Tic disorders can include fluctuating or intermittent expression. A clinician may describe current remission or very mild activity while retaining a history of a previous childhood-onset tic disorder.

Can tics come back after puberty?

Yes. Fluctuations can occur in adolescence and adulthood, even after an extended quiet period. A substantial new change still warrants clinical review, especially if the phenomenology differs from the earlier tics. The prognosis of reemerging childhood tics must be distinguished from entirely new adult-onset movements.

Are vocal tics less likely to go away than motor tics?

There is no clinically reliable rule by which the sound or movement type alone predicts an individual's remission. Motor and vocal tics can both change over time, and prognosis requires the broader history rather than a single observed tic. Specialist assessment is useful when the nature of a sound or movement is uncertain.

Does tic suppression make tics worse later?

Some individuals experience discomfort or changes in tic frequency around attempts to suppress, but a simple universal 'rebound' rule is not established for every person and situation. Suppression is a short-term behavioral phenomenon, while developmental prognosis is a long-term question. An individualized behavioral-treatment plan is preferable to forcing a person to suppress in every setting.

Can therapy make tics disappear permanently?

CBIT can meaningfully reduce tics and related interference for some people, but clinical guidelines do not promise permanent elimination. Natural remission and treatment-related improvement can overlap. Treatment choices should address current functional needs and be reviewed over time. AAN; ESSTS behavioral guidelines.

Do tics necessarily get worse when someone is anxious?

Some people have more tics during stress, fatigue, excitement, or transitions; others do not follow the same pattern. Anxiety can be a separate issue deserving care. Temporary environmental influence does not show that an underlying neurodevelopmental tic disorder was caused by anxiety. European assessment guideline.

Can a person with Tourette syndrome have a normal adult life?

Yes. Many people with Tourette syndrome study, work, develop relationships, and pursue their preferred activities. The relevant goal is participation and well-being, supported by clinical treatment or practical accommodations where needed. Persistent tics do not by themselves determine intellectual ability or adult prospects. The CDC overview describes wide variation in functioning and achievement.

The clinical bottom line

Childhood tics commonly improve during adolescence and early adulthood, and complete or near-complete remission occurs for some people. Persistent or severe adult tics remain possible, and current science cannot forecast an individual's trajectory with certainty. Good care therefore combines realistic long-term expectations with attention to the person's current comfort, participation, associated conditions, and preferences. A child deserves timely support during difficult years even if improvement is likely later.

References

Centers for Disease Control and Prevention. (2026). Data and statistics on Tourette syndrome. https://www.cdc.gov/tourette-syndrome/data/index.html

Centers for Disease Control and Prevention. (2026). About Tourette syndrome. https://www.cdc.gov/tourette-syndrome/about/index.html

Centers for Disease Control and Prevention. (2026). Diagnosing tic disorders. https://www.cdc.gov/tourette-syndrome/diagnosis/index.html

Centers for Disease Control and Prevention. (2026). Five things to know about Tourette syndrome. https://www.cdc.gov/tourette-syndrome/articles/five-things-about-tourette-syndrome.html

Centers for Disease Control and Prevention. (2026). Treatment of Tourette syndrome. https://www.cdc.gov/tourette-syndrome/treatment/index.html

Kim, S., Greene, D. J., Bihun, E. C., et al. (2019). Provisional tic disorder is not so transient. Scientific Reports, 9, 3951. https://doi.org/10.1038/s41598-019-40133-4

Bloch, M. H., & Leckman, J. F. (2009). Clinical course of Tourette syndrome. Journal of Psychosomatic Research, 67(6), 497–501. https://doi.org/10.1016/j.jpsychores.2009.09.002

Bloch, M. H., Peterson, B. S., Scahill, L., et al. (2006). Adulthood outcome of tic and obsessive-compulsive symptom severity in children with Tourette syndrome. Archives of Pediatrics & Adolescent Medicine, 160(1), 65–69. https://doi.org/10.1001/archpedi.160.1.65

Andrén, P., Jakubovski, E., Murphy, T. L., et al. (2022). European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part II: Psychological interventions. European Child & Adolescent Psychiatry, 31, 403–423. https://doi.org/10.1007/s00787-021-01845-z

Roessner, V., Eichele, H., Stern, J. S., et al. (2022). European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part III: Pharmacological treatment. European Child & Adolescent Psychiatry, 31, 425–441. https://doi.org/10.1007/s00787-021-01899-z

Pringsheim, T., Ganos, C., McGuire, J. F., et al. (2023). European Society for the Study of Tourette Syndrome 2022 criteria for clinical diagnosis of functional tic-like behaviours: International consensus from experts in tic disorders. European Journal of Neurology, 30, 902–910. https://doi.org/10.1111/ene.15672

Pringsheim, T., Okun, M. S., Müller-Vahl, K., et al. (2019). Practice guideline recommendations summary: Treatment of tics in people with Tourette syndrome and chronic tic disorders. Neurology, 92(19), 896–906. https://doi.org/10.1212/WNL.0000000000007466

Groth, C., Mol Debes, N., Rask, C. U., Lange, T., & Skov, L. (2017). Course of Tourette syndrome and comorbidities in a large prospective clinical study. Journal of the American Academy of Child & Adolescent Psychiatry, 56(4), 304–312. https://doi.org/10.1016/j.jaac.2017.01.010

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