Pascal and Francis Bibliographic Databases

Help

Search results

Your search

cc.\*:("002B22D")

Filter

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 12851

  • Page / 515
Export

Selection :

  • and

Neuronal cell death caused by inhibition of intracellular cholesterol trafficking is caspase dependent and associated with activation of the mitochondrial apoptosis pathwayZHILI HUANG; QINGSONG HOU; NAM SANG CHEUNG et al.Journal of neurochemistry. 2006, Vol 97, Num 1, pp 280-291, issn 0022-3042, 12 p.Article

Thérapies enzymatiques substitutives des maladies lysosomales = Enzyme replacement therapies for lysosomal storage disordersGERMAIN, Dominique P.MS. Médecine sciences. 2005, Vol 21, pp 77-83, issn 0767-0974, 7 p., NSArticle

Carnitine-acylcarnitine translocase deficiency: case report and review of the literatureRUBIO-GLOZALBO, M. E; VOS, P; FORGET, Pph et al.Acta paediatrica (Oslo). 2003, Vol 92, Num 4, pp 501-504, issn 0803-5253, 4 p.Article

Vitamin C therapy ameliorates vascular endothelial dysfunction in treated patients with homocystinuriaPULLIN, C. H; BONHAM, J. R; MCDOWELL, I. F. W et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 2, pp 107-118, issn 0141-8955Article

Niemann-Pick disease type C in adultsIMRIE, J; VIJAYARAGHAVEN, S; WHITEHOUSE, C et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 6, pp 491-500, issn 0141-8955, 10 p.Article

La maladie de Gaucher chez l'enfant : mode de révélation, évolution naturelle, apports du traitement par l'enzyme de remplacement = Gaucher's disease in children: first clinical signs, natural course and benefits of enzyme replacement therapyCAUBEL, I; DE VILLEMEUR, T. Billette; BELMATOUG, N et al.Archives de pédiatrie (Paris). 2003, Vol 10, Num 8, pp 681-688, issn 0929-693X, 8 p.Article

Sandhoff disease in a golden retriever dogYAMATO, O; MATSUKI, N; SATOH, H et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 4, pp 319-320, issn 0141-8955Article

Glutaric aciduria type III: A distinctive non-disease?KNERR, I; ZSCHOCKE, J; HOFFMANN, G. F et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 6, pp 483-490, issn 0141-8955, 8 p.Article

Mutation analysis of the acid ceramidase gene in Japanese patients with Farber diseaseMURAMATSU, T; SAKAI, N; YANAGIHARA, I et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 7, pp 585-592, issn 0141-8955, 8 p.Article

Carbohydrate-deficient glycoprotein syndromes : inborn errors of protein glycosylationKEIR, G; WINCHESTER, B. G; CLAYTON, P et al.Annals of clinical biochemistry. 1999, Vol 36, pp 20-36, issn 0004-5632, 1Article

Hepatocellular transplantation in rats with congenital ascorbic acid deficiencyONODERA, K; KASAI, S; MITO, M et al.Nippon Geka Gakkai Zasshi. 1995, Vol 96, Num 5, pp 301-308, issn 0301-4894Article

Effects of Cl channel blockers on Ca-activated chloride and potassium currents in smooth muscle cells from rabbit portal veinHOGG, R. C; WANG, Q; LARGE, W. A et al.British journal of pharmacology. 1994, Vol 111, Num 4, pp 1333-1341, issn 0007-1188Article

Relative efficiency of incorporation of newly synthesized elastin and collagen into aorta, pulmonary artery and pulmonary vein of growing pigsJOHNSON, D. J; LABOURENE, J; RABINOVITCH, M et al.Connective tissue research (Print). 1993, Vol 29, Num 3, pp 213-221, issn 0300-8207Conference Paper

Fabry's disease with complete atrioventricular block : histological evidence of involvement of the conduction systemIKARI, Y; KUWAKO, K; YAMAGUCHI, T et al.British heart journal. 1992, Vol 68, Num 3, pp 323-325, issn 0007-0769Article

Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiencyDAVIDSON-MUNDT, A; LUDER, A. S; GREENE, C. L et al.The Journal of pediatrics. 1992, Vol 120, Num 3, pp 444-446, issn 0022-3476Article

DNA ploidy abnormalities in the liver of children with hereditary tyrosinemia type I : correlation with histopathologic featuresZERBINI, C; WEINBERG, D. S; HOLLISTER, K. A et al.The American journal of pathology. 1992, Vol 140, Num 5, pp 1111-1119, issn 0002-9440Article

Arachidonic acid- and acetylcholine-induced relaxations of rabbit aortaPFISTER, S. L; CAMPBELL, W. B.Hypertension (Dallas, Tex. 1979). 1992, Vol 20, Num 5, pp 682-689, issn 0194-911XArticle

Pertussis toxin reduces endothelium-dependent and idependent responses to alpha-2 adrenergic stimulation in systemic canine arteries and veinsMILLER, V. M; FLAVAHAN, N. A; VANHOUTTE, P. M et al.The Journal of pharmacology and experimental therapeutics. 1991, Vol 257, Num 1, pp 290-293, issn 0022-3565, 4 p.Article

Clinical presentation and natural course of the carbohydrate-deficient glycoprotein syndromeJAEKEN, J; HAGBERG, B; STRØMME, P et al.Acta paediatrica Scandinavica. Supplement. 1991, Num 375, pp 6-13, issn 0300-8843Conference Paper

Conférences/Journée scientifique sur «Les maladies héréditaires du métabolisme. Du dépistage à la biologie moléculaire», Paris, 13 novembre 1987 = Conferences/Inborn errors of metabolism. From screening to molecular biology scientific meeting. Paris, November 13, 1987Annales de biologie clinique (Paris). 1988, Vol 46, Num 6, pp 381-405, issn 0003-3898Conference Proceedings

Epoxy acids in peroxisomal disordersSTOKKE, O; JELLUM, E; KVITTINGEN, E. A et al.Scandinavian journal of clinical & laboratory investigation. 1986, Vol 46, Num 1, pp 95-96, issn 0036-5513Article

Heritable metabolic storage diseasesGEBHART, W.Journal of cutaneous pathology. 1985, Vol 12, Num 3-4, pp 348-357, issn 0303-6987Article

Blood cells as markers for metabolic disordersBEUTLER, E.Blut. 1985, Vol 51, Num 6, pp 371-376, issn 0006-5242Article

Metabolische Myopathien im Kindesalter i eine Übersicht in kurzgefasster Form = Myopathies métaboliques chez le nourrisson et l'enfant: brève revue = Metabolic myopathies in infancy and childhood. A concise reviewSCHAUB, J.Monatsschrift für Kinderheilkunde. 1984, Vol 132, Num 8, pp 566-573, issn 0026-9298Article

Metabolische Myopathien = Myopathies métaboliques = Metabolic myopathiLÖSSNER, J; KÜHN, H. J.Psychiatrie, Neurologie und medizinische Psychologie. 1984, Vol 36, Num 9, pp 513-526, issn 0033-2739Article

  • Page / 515