PART 4 in Microsoft Office

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PART 4
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MAJOR CATEGORIES OF NEUROLOGIC DISEASE
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NISHIMURA M, YOSHIMO K, TOMITA Y: Central and peripheral nervous system pathology due to methylenetetrahydrofolate reductase de ciency Pediatr Neurol 1:375, 1985 NYGAARD TG, MARSDEN CD, FAHN S: Dopa-responsive dystonia: Longterm treatment response and prognosis Ann Neurol 35:396, 1994 OETTING WS, KING RA: Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism Hum Mutat 13:99, 1999 OHNO T, TSUCHIDA H, FUKUHARA N, et al: Adrenoleukodystrophy: A clinical variant presenting as olivopontocerebellar atrophy J Neurol 231: 167, 1984 OHTAHARA S: Seizure disorders in infancy and childhood Brain Dev 6: 509, 1984 PASTORES GM, THADHANI R: Enzyme-replacment therapy for AndersonFabry disease Lancet 358:601, 2001 PAVLAKIS SG, PHILLIPS PC, DIMAURO S, et al: Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: A distinctive clinical syndrome Ann Neurol 16:481, 1984 PINCUS JH, CHUTORIAN A: Familial benign chorea with intention tremor: A clinical entity J Pediatr 70:724, 1967 PRADER A, LABHART A, WILLI H: Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter Schweiz Med Wochenschr 86:1260, 1956 PRANZATELLI MR, HUANG Y, TATE E, et al: Cerebrospinal uid 5-hydroxy indoleacetic acid in the pediatric opsoclonus-myoclonus syndrome Ann Neurol 37:189, 1995 PRECHTL H, BEINTEMA D: The Neurological Examination of the FullTerm Newborn Infant London, Spastics Society, 1964 PRENSKY AL, MOSER HW: Brain lipids, proteo-lipids and free amino acids in maple syrup urine disease J Neurochem 13:863, 1966 RAPIN I, GOLDFISCHER S, KATZMAN R, et al: The cherry-red spotmyoclonus syndrome Ann Neurol 3:134, 1978 ROBITAILLE Y, CARPENTER S, KARPATI G, et al: A distinct form of adult polyglycosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes Brain 103:315, 1980 ROPPER AH, HATTEN HP, DAVIS KR: Computed tomography in Wilson disease: Report of two cases Ann Neurol 5:102, 1979 ROSENBERG AL, BERGSTROM L, TROOST BT, BARTHOLOMEW BA: Hyperuricemia and neurologic de cits: A family study N Engl J Med 282: 992, 1970 ROSENBERG LE, SCRIVER CR: Disorders of amino acid metabolism, in Bondy PK, Rosenberg LE (eds): Metabolic Control and Disease, 8th ed Philadelphia, Saunders, 1980, pp 583 776 ROWE PC, NEWMAN SL, BRUSILOW SW: Natural history of symptomatic partial ornithine transcarbamylase de ciency N Engl J Med 314:541, 1986 SAATCI I, TOPCU M, BALTAOGLU FF, et al: Cranial MRI ndings in Wilson s disease Acta Radiol 38:250, 1997 SALEM M: Metabolic ataxias, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology Vol 21 Amsterdam, North-Holland, 1975, pp 573 585 SANSARICQ C, LYON G, KOLODNY EH: Seizures in hereditary metabolic disease: Evaluation of suspected hereditary metabolic disease in the etiology of seizures, in Kotogal P, Luders H (eds): The Epilepsies: Etiologies and Prevention San Diego, CA, Academic Press, 1999, pp 457 464 SANTAVUORI P, HALTIA M, RAPOLA J, RAITTA C: Infantile type of socalled neuronal ceroid-lipofuscinosis: Part 1 A clinical study of 15 patients J Neurol Sci 18:257, 1973 SANTORELLI F, SHANSKE S, MACAY A, et al: The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh s syndrome Ann Neurol 34:827, 1994 SAVOIARDO M, HALLIDAY WC, NARDOCCI N, et al: Hallervorden-Spatz disease: MR and pathologic ndings AJNR 14:155, 1993 SCHAPIRA AH, DIMAURO S(eds): Mitochondrial Disorders in Neurology Oxford, England, Butterworth-Heinemann, 1994
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SCHEINBERG IH, GITLIN D: De ciency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson s disease) Science 116:484, 1952 SCHEINBERG IH, STERNLIEB I: Wilson s Disease: Major Problems in Internal Medicine Vol 23 Philadelphia, Saunders, 1984 SCHILSKY ML, SCHEINBERG IH, STERNLIEB I: Liver transplantation for Wilson s disease: Indications and outcome Hepatology 19:583, 1994 SCRIVER CR, BEAUDET AL, SLY WS, VALLE D (eds): The Metabolic and Molecular Bases of Inherited Disease, 7th ed New York, McGraw-Hill, 1995 SCRIVER CR, CLOW CL: Phenylketonuria: Epitome of human biochemical genetics N Engl J Med 303:1335, 1980 SEITELBERGER F: Pelizaeus-Merzbacher disease, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology Vol 10 Amsterdam, NorthHolland, 1970, pp 150 202 SETHI KD, RAY R, ROESEL RA, et al: Adult-onset chorea and dementia with propionic acidemia Neurology 39:1343, 1989 SHAFFNER JM, WALLACE DC: Oxidative phosphorylation diseases, in Scriver CR, Beaudet AL, Sly WS, Valle D (eds): The Metabolic and Molecular Bases of Inherited Disease, 7th ed New York, McGraw-Hill, 1995, pp 1535 1609 SHIH VE, ABRAMS IF, JOHNSON JL, et al: Sul te oxidase de ciency N Engl J Med 297:1022, 1977 SHIH VE, SAFRAN AP, ROPPER AH, TUCHMAN M: Ornithine carbamoyl transferase de ciency: Unusual clinical ndings and novel mutation J Inherit Metab Dis 22:672, 1999 SHUMAN RM, LEECH RW, SCOTT CR: The neuropathology of the nonketotic and ketotic hyperglycinemias: Three cases Neurology 28:139, 1978 SHY GM, GONATAS NK, PEREZ M: Two childhood myopathies with abnormal mitochondria: I Megaconial myopathy II Pleoconial myopathy Brain 89:133, 1966 SIEMERLING E, CREUTZFELDT HG: Bronzekrankheit und sklerosierende encephalomyelitis (diffuse sklerose) Arch Psychiatr Nervenkr 68:217, 1923 SJOGREN T: Die juvenile amaurotische Idiotie: Klinische und erblichkeitsmedizinische Untersuchungen Hereditas 14:197, 1931 SLY WS, WHYTE MP, SUNDERAM V: Carbonic anhydrase II de ciency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis with cerebral calci cation N Engl J Med 313: 139, 1985 STABA SL, ESCOLAR ML, POE M, et al: Cord-blood transplants from unrelated donors in patients with Hurler s syndrome N Eng J Med 350: 1960, 2004 STAROSTA-RUBINSTEIN S, YOUNG AB, KLUIN K, et al: Clinical assessment of 31 patients with Wilson s disease Arch Neurol 44:365, 1987 STRICH SJ: Pathological ndings in three cases of ataxia-telangiectasia J Neurol Neurosurg Psychiatry 29:489, 1966 STUMPF E, MASSON H, DUQUETTE A, et al: Adult Alexander disease with autosomal dominant transmission Arch Neurol 60:1307, 2003 SWOBODA KJ, SAUL JP, MCKENNA CE, et al: Aromatic L-amino acid decarboxylase de ciency Overview of clinical features and outcomes Ann Neurol 54(Suppl 6):S49, 2000 SZANTO J, GALLYAS F: A study of iron metabolism in neuropsychiatric patients: Hallervorden-Spatz disease Arch Neurol 14:438, 1966 TAGAWA A, ONO S, SHIBATA M, et al: A new neurological entity manifesting as involuntary movements and dysarthria with possible abnormal copper metabolism J Neurol Neurosurg Psychiatry 71:780, 2001 TAIVASSALO T, ABBOTT A, WYRICK P, et al: Venous oxygen levels during aerobic exercise: An index of impaired oxidative metabolism in mitochondrial myopathy Ann Neurol 51:38, 2002 TASSINARI CA, MICHELUCCI R, GENTON P, et al: Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): A condition unrelated to mitochondrial encephalomyopathies J Neurol Neurosurg Psychiatry 52: 262, 1989
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