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Robin sequence: from diagnosis to development of an effective management plan

Pediatrics (Evanston), 2011-05, Vol.127 (5), p.936

2011

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Best Practices for the Diagnosis and Evaluation of Infants With Robin Sequence: A Clinical Consensus Report

JAMA pediatrics, 2016-09, Vol.170 (9), p.894

2016

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The Tübingen palatal plate approach to Robin sequence: Summary of current evidence

Journal of cranio-maxillo-facial surgery, 2019-11, Vol.47 (11), p.1699-1705

2019

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Underlying Genetic Diagnosis of Pierre Robin Sequence: Retrospective Chart Review at Two Children’s Hospitals and a Systematic Literature Review

The Journal of pediatrics, 2012-04, Vol.160 (4), p.645-650.e2

2012

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Congenital talipes equinovarus (clubfoot)

American journal of obstetrics and gynecology, 2019-12, Vol.221 (6), p.B10-B12

2019

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Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies

Muscle & nerve, 2021-04, Vol.63 (4), p.516-524

2021

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Genetics of craniofacial malformations

Seminars in fetal & neonatal medicine, 2021-12, Vol.26 (6), p.101290-101290, Article 101290

2021

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Syndromes associated with Robin sequence: a national prospective cohort study

Archives of disease in childhood, 2023-01, Vol.108 (1), p.42

2023

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European Guideline Robin Sequence An Initiative From the European Reference Network for Rare Craniofacial Anomalies and Ear, Nose and Throat Disorders (ERN-CRANIO)

The Journal of craniofacial surgery, 2024-01, Vol.35 (1), p.279

By the Working Group on Writing a European Guideline on Robin Sequence

2024

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The management of upper airway obstruction in Pierre Robin Sequence

Paediatric respiratory reviews, 2023-03, Vol.45, p.11-15

2023

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Robin sequence without cleft palate: Genetic diagnoses and management implications

American journal of medical genetics. Part A, 2022-01, Vol.188 (1), p.160-177

2022

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Global birth prevalence of Robin sequence in live-born infants: a systematic review and meta-analysis

European respiratory review, 2023-12, Vol.32 (170), p.230133

2023

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Outcomes Analysis of Mandibular Distraction Osteogenesis for the Treatment of Pierre Robin Sequence

Plastic and reconstructive surgery (1963), 2013-08, Vol.132 (2), p.419-421

2013

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Screening for Obstructive Sleep Apnea and Associated Risk Factors in Adolescents and Adults With Isolated Robin Sequence

The Cleft palate-craniofacial journal, 2024-01, Vol.61 (1), p.79-86

2024

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A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report

Medicine (Baltimore), 2020-11, Vol.99 (45), p.e23033

2020

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Clinical, cytogenetic, and molecular outcomes in a series of 66 patients with Pierre Robin sequence and literature review: 22q11.2 deletion is less common than other chromosomal anomalies

American journal of medical genetics. Part A, 2016-04, Vol.170A (4), p.870-880

2016

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Objective measurements for upper airway obstruction in infants with Robin sequence: what are we measuring? A systematic review

Journal of clinical sleep medicine, 2021-08, Vol.17 (8), p.1717-1729

2021

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Differences in analysis and treatment of upper airway obstruction in Robin sequence across different countries in Europe

European journal of pediatrics, 2023-03, Vol.182 (3), p.1271-1280

2023

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DDX3X mutations in two girls with a phenotype overlapping Toriello–Carey syndrome

American journal of medical genetics. Part A, 2017-05, Vol.173 (5), p.1369-1373

2017

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Pierre Robin sequence: Review of diagnostic and treatment challenges

International journal of pediatric otorhinolaryngology, 2015-04, Vol.79 (4), p.451-464

2015

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Pierre Robin Sequence: A Perioperative Review

Anesthesia and analgesia, 2014-08, Vol.119 (2), p.400-412

2014

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First reported adult patient with TARP syndrome: A case report

American journal of medical genetics. Part A, 2018-12, Vol.176 (12), p.2915-2918

2018

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Outcomes of Cleft Palate Repair in Patients with Pierre Robin Sequence: A Matched Case-Control Study

Plastic and reconstructive surgery (1963), 2016-03, Vol.137 (3), p.927-935

2016

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Catel–Manzke syndrome without Manzke dysostosis

American journal of medical genetics. Part A, 2020-03, Vol.182 (3), p.437-440

2020

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Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence

Human molecular genetics, 2014-05, Vol.23 (10), p.2569-2579

2014

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Robin sequence: from diagnosis to development of an effective management plan

Best Practices for the Diagnosis and Evaluation of Infants With Robin Sequence: A Clinical Consensus Report

The Tübingen palatal plate approach to Robin sequence: Summary of current evidence

Underlying Genetic Diagnosis of Pierre Robin Sequence: Retrospective Chart Review at Two Children’s Hospitals and a Systematic Literature Review

Congenital talipes equinovarus (clubfoot)

Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies

Genetics of craniofacial malformations

Syndromes associated with Robin sequence: a national prospective cohort study

European Guideline Robin Sequence An Initiative From the European Reference Network for Rare Craniofacial Anomalies and Ear, Nose and Throat Disorders (ERN-CRANIO)

The management of upper airway obstruction in Pierre Robin Sequence

Robin sequence without cleft palate: Genetic diagnoses and management implications

Global birth prevalence of Robin sequence in live-born infants: a systematic review and meta-analysis

Outcomes Analysis of Mandibular Distraction Osteogenesis for the Treatment of Pierre Robin Sequence

Screening for Obstructive Sleep Apnea and Associated Risk Factors in Adolescents and Adults With Isolated Robin Sequence

A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report

Clinical, cytogenetic, and molecular outcomes in a series of 66 patients with Pierre Robin sequence and literature review: 22q11.2 deletion is less common than other chromosomal anomalies

Objective measurements for upper airway obstruction in infants with Robin sequence: what are we measuring? A systematic review

Differences in analysis and treatment of upper airway obstruction in Robin sequence across different countries in Europe

DDX3X mutations in two girls with a phenotype overlapping Toriello–Carey syndrome

Pierre Robin sequence: Review of diagnostic and treatment challenges

Pierre Robin Sequence: A Perioperative Review

First reported adult patient with TARP syndrome: A case report

Outcomes of Cleft Palate Repair in Patients with Pierre Robin Sequence: A Matched Case-Control Study

Catel–Manzke syndrome without Manzke dysostosis

Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence

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