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Publications by John B. Winer
Clinical and Myopathological Characteristics of Desminopathy Caused by a Mutation in Desmin Tail Domain
European Neurology
Neurology
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Familial Scaphocephaly Syndrome Caused by a Novel Mutation in the FGFR2 Tyrosine Kinase Domain
Journal of Medical Genetics
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Characteristics and Clinical Course of Dysphagia Caused by Anterior Cervical Osteophyte
Annals of Rehabilitation Medicine
Rehabilitation
Desmin Mutation Responsible for Idiopathic Dilated Cardiomyopathy
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Congenital Long-Qt Syndrome Caused by a Novel Mutation in a Conserved Acidic Domain of the Cardiac Na+ Channel
Circulation
Cardiovascular Medicine
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Epilepsy in 11 Patients With Typical Rett Syndrome Caused by Mecp2 Mutation: Clinical and Electroencephalographic Characteristics, Course, Therapy (Results of the Authors’ Observations)
Russkii Zhunal Detskoi Nevrologii
Child Health
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Pediatrics
Perinatology
The Clinical Characteristics of Tumours and the Shock Caused by Surgical Operations
BMJ
Clinical and Genetic Analysis of ZTTK Syndrome Caused by SON Heterozygous Mutation C.394C>T
Molecular genetics & genomic medicine
Genetics
Molecular Biology
RelA Functionally Suppresses the Growth Defect Caused by a Mutation in the G Domain of the Essential Der Protein
Journal of Bacteriology
Microbiology
Molecular Biology
Recurrent Inflammatory Disease Caused by a Heterozygous Mutation in CD48
Journal of Allergy and Clinical Immunology
Allergy
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