Myhre syndrome: Clinical features and restrictive cardiopulmonary complications
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Myhre syndrome: Clinical features and restrictive cardiopulmonary complications
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 167, Issue 12, Pages 2893-2901
Publisher
Wiley
Online
2015-09-30
DOI
10.1002/ajmg.a.37273
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Myhre-LAPs syndrome and intubation related airway stenosis: keys to diagnosis and critical therapeutic interventions
- (2015) Michael S. Oldenburg et al. AMERICAN JOURNAL OF OTOLARYNGOLOGY
- Myhre syndrome with facial paralysis and branch pulmonary stenosis
- (2015) Lara Hawkes et al. CLINICAL DYSMORPHOLOGY
- NovelSMAD4mutation causing Myhre syndrome
- (2014) Viviana Caputo et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Myhre syndrome
- (2014) C. Le Goff et al. CLINICAL GENETICS
- Myhre syndrome: a rare craniofacial disorder
- (2014) Naho Ishibashi et al. CRANIO-THE JOURNAL OF CRANIOMANDIBULAR PRACTICE
- Myhre and LAPS syndromes: clinical and molecular review of 32 patients
- (2014) Caroline Michot et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- SMAD4 mutations causing Myhre syndrome result in disorganization of extracellular matrix improved by losartan
- (2014) Pasquale Piccolo et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Bilateral Otospongiosis and a Unilateral Vestibular Schwannoma in a Patient With Myhre Syndrome
- (2014) Christoph Kenis et al. OTOLOGY & NEUROTOLOGY
- Recurrent Pericarditis in Myhre Syndrome
- (2013) Paolo Picco et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome
- (2012) Viviana Caputo et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations of SMAD4 account for both LAPS and Myhre syndromes
- (2012) Noralane M. Lindor et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- First case of a Japanese girl with Myhre syndrome due to a heterozygousSMAD4mutation
- (2012) Yumi Asakura et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- From tall to short: The role of TGFβ signaling in growth and its disorders
- (2012) Carine Le Goff et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Retinal involvement in two unrelated patients with Myhre syndrome
- (2012) Essam Al Ageeli et al. European Journal of Medical Genetics
- Smad4 disruption accelerates keratinocyte reepithelialization in murine cutaneous wound repair
- (2012) Leilei Yang et al. HISTOCHEMISTRY AND CELL BIOLOGY
- Myhre syndrome with ataxia and cerebellar atrophy
- (2011) Ruxandra Bachmann-Gagescu et al. CLINICAL DYSMORPHOLOGY
- Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome
- (2011) Carine Le Goff et al. NATURE GENETICS
- A new growth deficiency syndrome
- (2010) Selma A. Myhre et al. CLINICAL GENETICS
- LAPS syndrome and Myhre syndrome: Two disorders or one?
- (2009) Noralane M. Lindor AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Atrial fibrosis and atrial fibrillation: The role of the TGF-β1 signaling pathway
- (2009) Felix Gramley et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation