Mucosulfatidosis. Study of 3 familial cases
Couchot, J.; Pluot, M.; Schmauch, M.A.; Pennaforte, F.; Fandre, M.
Archives Francaises de Pediatrie 31(8): 775-795
1974
ISSN/ISBN: 0003-9764 PMID: 4218948 Document Number: 76042
Document emailed within 1 workday
Related Documents
Baroncelli, P.G.; Crua, G.; Balocco, A. 1971: Gastroduodenal ulcer in the evolutive age. Study of 6 cases, including 3 familial cases Archivio Per le Scienze Mediche 128(3): 120-131Naffah, J.; Bitar, E.; Nasr, W.; Khoury, K. 1975: Gentic study of paroxystic familial polyseritis. 72 cases La Nouvelle Presse Medicale 4(14): 1031-1033
Vasant, A.; Taly, A.B.; Sathynarayanaswamy, H. 1994: Limb girdle myasthenia: a study of familial and sporadic cases Journal of the Association of Physicians of India 42(8): 601-603
Petit, A.; Dupont, B.; Sansonetti, P.; Raffoux, C.; Lapresle, C. 1983: Horton's disease. Study of HLA group. Apropos of 3 familial cases Presse Medicale 12(40): 2536
Boudouresques, J.; Roger, J.; Khalil, R.; Pellissier, J.F.; Ali-Cherif, A.; Tafani, B.; Champion, M.F. 1978: 2 familial cases of Lafora disease. Clinical, electroencephalographic and pathologic study Revue Neurologique (Paris) 134(8-9): 523-540
Mrabet, A.; Oueslati, S.; Gazzah, H.; Ben Hamida, M. 1991: Clinical and electrophysiological study of 2 familial cases of Marcus Gunn phenomenon Revue Neurologique (Paris) 147(3): 215-219
Stringa, O.J.; Bianchi, C.A.; Stringa, S.G.; Bianchi, O. 1985: Chronic benign familial pemphigus. Clinical, histological and immunological study of 7 cases Medicina Cutanea Ibero-Latino-Americana 13(4): 281-289
Kone-Paut, I.; Uring-Lambert, B.; Berbis, P.; Goldstein, M.M.; Palix, C.; Bernard, D.; Hauptmann, G.; Bernard, J.L. 1992: Cold urticaria, cutaneous vasculitis and C4B homozygote deficiency. Apropos of 2 cases with a familial study Archives Francaises de Pediatrie 49(Suppl 1): 245-248
Dhondt, J.L.; Mesmacque-Caby, D.; Farriaux, J.P.; Fontaine, G. 1972: Diagnostic and therapeutic problems of phenylketonuria. Parallel study of 2 familial cases as a function of treatment Lille Medical: Journal de la Faculte de Medecine et de Pharmacie de l'Universite de Lille 17(10): 1432-1436
Miyanaga, O.; Shirahama, M.; Ishibashi, H. 1990: A study of familial case histories of hepatocellular carcinoma--285 cases in Saga Prefectural Hospital Gan no Rinsho. Japan Journal of Cancer Clinics 36(2): 127-131
Cavallari, V.; Di Pasquale, M.R.; Scuderi, D. 1981: Hereditary neuropathy with a tendency to compression paralysis. Electrophysiological, morphometric and ultrastructural study of 2 familial cases Acta Neurologica 3(1): 187-196
Broussolle, E.; Defuentes, G.; Plauchu, H.; Chazot, G. 1997: Incidence and clinical profile of familial forms of Parkinson's disease. A study of 428 index-cases from a department of neurology Revue Neurologique (Paris) 153(6-7): 406-411
Poissonnier, M.; Andrieu, J.; Gardon, J.D.; Saint-Martin, J.L.; Gruyer, P.; Martignon, C. 1983: Familial cancer of the colon without polyposis and the familial cancer syndrome. Apropos of 2 cases over 3 generations Journal de Genetique Humaine 31(4): 255-278
Pasquier, B.; Couderc, P.; Tommasi, M.; Groslambert, R.; Pasquier, D. 1975: Association of multiple basal cell carcinomas of the face and spinocerebellar degeneration. Study of 4 familial cases including an anatomo-clinical description La semaine des hopitaux: organe fonde par l'Association d'enseignement medical des hopitaux de Paris 51(49): 3009-3017
Remacha, A.F.; del Río, E.; Baiget, M. 1998: Atypical familial microcytosis: a familial and genetic study Medicina Clinica 110(5): 183-185
Vilotte, J.; Bonstein, U.; Girodet, J.; De Mestier du Bourg, P.; Mignon, M.; Bonfils, S. 1989: Familial colonic cancer (Lynch's syndrome) and bile duct cancer. Study of 2 cases Gastroenterologie Clinique et Biologique 13(12): 1072-1074
Turleau, C.; de Grouchy, J.; Chavin-Colin, F.; Despoisses, S.; Leblanc, A. 1983: Two cases of del(13q)-retinoblastoma and two cases of partial trisomy due to a familial insertion Annales de Genetique 26(3): 158-160
Peirone, F.; Spada, A. 1972: 2 cases of familial monilethrix Minerva Medica 63(4): 272-278
Roy, C. 1977: Familial pseudohypoaldosteronism (apropos of 5 cases) Archives Francaises de Pediatrie 34(1): 37-54
Wu, Y.T. 1993: Familial cherubism (report of 10 cases) Zhonghua Kou Qiang Yi Xue Za Zhi 28(3): 148-50 190-1