Mohammed Tredano

Mutation of <i>SFTPC</i> in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease

Mohammed Tredano, Matthias Griese, Frank Brasch et al. · American Journal of Medical Genetics Part A · 2004 · 142 citations

Pulmonary Surfactant, Inflammatory Lung Disease, Advanced Lung Disease +16

Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: Relationship to <i>SFTPB</i>

Mohammed Tredano, Matthias Griese, J. de Blic et al. · American Journal of Medical Genetics Part A · 2003 · 55 citations

Neonatology, Respiratory Distress Syndrome (Pulmonary Critical Care), Pediatric Cases +20

CompoundSFTPB 1549C?GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency

Mohammed Tredano, Ruurd M. van Elburg, Ageeth Kaspers et al. · Human Mutation · 1999 · 53 citations

<i>FOXC2</i> truncating mutation in distichiasis, lymphedema, and cleft palate

Michel Bahuau, Claude Houdayer, Mohammed Tredano et al. · Clinical Genetics · 2002 · 38 citations

Mendelian Disorder, Autoimmune Disease, Ophthalmology +13

Origin of the prevalent <i>SFTPB</i> indel g.1549C &gt; GAA (121ins2) mutation causing surfactant protein B (SP‐B) deficiency

Mohammed Tredano, D.N. Cooper, Manfred Stuhrmann et al. · American Journal of Medical Genetics Part A · 2005 · 25 citations