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Showing articles 0 to 10 of 10 Filter Applied: short stature (Click to remove) Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever Neurol 102:e209358, Barbosa,A.R.,et al, 2024 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Extraintestinal Manifestations of Coeliac Disease Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015 Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification NEJM 313:139-181, Sly,W.S.,et al, 1985 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Germinoma of third Ventricle (Case Record of MGH) NEJM 293:653, Locke,S.,et al, 1975 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue (Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972 Morquio's Disease, A Radiologic & Morphologic Study Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964 Showing articles 0 to 10 of 10