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Showing articles 0 to 12 of 12 Filter Applied: skin,biopsy (Click to remove) A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Mucolipidosis Type IV; Characteristic MRI Findings Neurol 51:565-569, Frei,K.P.,et al, 1998 Clinical Pathological Conference Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978 Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria Neurol 52:1472-1478, Nardocci,N.,et al, 1999 X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample Ann Neurol 42:249-253, Mora,M.,et al, 1997 Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy Lancet 347:582-584, Sewry,C.A.,et al, 1996 Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature Angiology 38:769-784, Fine,M.J.,et al, 1987 An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981 Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980 Pseudoxanthoma Elasticum:A Review of Neurological Complications Ann Neurol 4:18, Iqbal,A.,et al, 1978 Showing articles 0 to 12 of 12