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Showing articles 0 to 12 of 12 Filter Applied: hepatomegaly (Click to remove) Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992 Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis NEJM 385:1220-1229, Case 29-2021, 2021 Wilson Disease Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016 Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis UptoDate Oct. 2014, McClain, K.L., 2014 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Wilson Disease:Clinical Presentation, Treatment, and Survival Ann Int Med 115:720-726, Stremmel,W.,et al, 1991 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Neurological Complications of Infantile Osteopetrosis Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977 Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients Medicine 55:467, Knox,D.L.,et al, 1976 The Natural History of SLE by Prospective Analysis Medicine 50:85, Estes,D.,et al, 1971 Showing articles 0 to 12 of 12