Raziel Lurie

Autosomal Recessive Ichthyosis with Hypotrichosis Caused by a Mutation in ST14, Encoding Type II Transmembrane Serine Protease Matriptase

Lina Basel‐Vanagaite, Revital Attia, Akemi Ishida‐Yamamoto et al. · The American Journal of Human Genetics · 2007 · 188 citations · Full text

Autosomal Recessive Ichthyosis, Medicine, Genetics +5

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin

Eli Sprecher, Gabriele Richard, Raziel Lurie et al. · Nature Genetics · 2001 · 184 citations

Ocular Disease, Ophthalmology, Pathology +5

A Missense Mutation in CDH3, Encoding P-Cadherin, Causes Hypotrichosis with Juvenile Macular Dystrophy

Margarita Indelman, Danny Petronius, Dan Ciubutaro et al. · Journal of Investigative Dermatology · 2002 · 67 citations · Full text

Ocular Disease, Encoding P-cadherin, Ophthalmology +8

Esophageal involvement in pemphigus vulgaris: A clinical, histologic, and immunopathologic study

Akiva Trattner, Raziel Lurie, A Leiser et al. · Journal of the American Academy of Dermatology · 1991 · 59 citations

Esophagus, Allergy, Medicine +5

Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy

Margarita Indelman, Michal Ramon, Eli Sprecher et al. · Journal of Investigative Dermatology · 2003 · 50 citations · Full text

Phenotypic Diversity, Ocular Disease, Ophthalmology +6