Ralph Lachman

Enzyme-Replacement Therapy in Mucopolysaccharidosis I

Emil Kakkis, Joseph Muenzer, George E. Tiller et al. · New England Journal of Medicine · 2001 · 675 citations · Full text

Life Sciences, Biochemistry, Genetics +11

Nosology and classification of genetic skeletal disorders: 2015 revision

Luisa Bonafé, Valérie Cormier‐Daire, Christine M Hall et al. · American Journal of Medical Genetics Part A · 2015 · 565 citations

Life Sciences, Genetics, Molecular Genetics +15

Kasabach-Merritt Syndrome-Associated Kaposiform Hemangioendothelioma Successfully Treated With Cyclophosphamide, Vincristine, and Actinomycin D

Bing Hu, Ralph Lachman, Jeffery Phillips et al. · Journal of Pediatric Hematology/Oncology · 1998 · 86 citations

Medicine, Oncology, Surgery +14

Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: Delineation of a new entity and review of lethal forms of multiple pterygium syndrome

H. Chen, LaDonna Immken, Ralph Lachman et al. · American Journal of Medical Genetics · 1984 · 83 citations

Medicine, Maxillofacial Radiology, Cystic Lesions Of The Jaws +16

Radiologic and neuroradiologic findings in the mucopolysaccharidoses

Ralph Lachman, Kenneth W. Martin, Sérgio Castro et al. · Journal of Pediatric Rehabilitation Medicine · 2010 · 76 citations · Full text

Medicine, Neurology, Radiology +17