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La maladie de gaucher type 1 : à propos de deux observations chez l'adulteHADHRI, R; HMISSA, S; KORBI, S et al.MHA (Sousse). 2005, Vol 17, Num 48, pp 66-68, issn 0330-8030, 3 p.Article

Rapid molecular weight determination for native glucocerebrosidase from human placenta using high-performance liquid chromatographySTRASBERG, P. M; LOWDEN, J. A.Journal of chromatography. 1983, Vol 261, Num 3, pp 419-422, issn 0021-9673Article

THE EFFECT OF A HEAST-STABLE FACTOR IN HUMAN SPLEEN ON GLUCOCEREBROSIDASE AND ACID BETA -GLUCOSIDASE ACTIVITIESPENTCHEV PG; BRADY RO.1973; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1973; VOL. 297; NO 2; PP. 491-496; BIBL. 7REF.Serial Issue

Structure of the N-asparagine-linked oligosaccharide units of human placental β-glucocerebrosidaseTAKASAKI, S; MURRAY, G. J; FURBISH, F. S et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 16, pp 10112-10117, issn 0021-9258Article

Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cellsMCNEILL, Alisdair; MAGALHAES, Joana; SCHAPIRA, Anthony H. V et al.Brain. 2014, Vol 137, pp 1481-1495, issn 0006-8950, 15 p., 5Article

Les manifestations neurologiques de la maladie de Gaucher de type 1: vers une remise en cause de la classification actuelle ? = Neurological manifestations of type 1 Gaucher's disease : Is a revision of disease classification needed?CHERIN, P; SEDEL, F; MIGNOT, C et al.Revue neurologique (Paris). 2006, Vol 162, Num 11, pp 1076-1083, issn 0035-3787, 8 p.Article

Successful treatment of bone marrow failure in Gaucher's disease with low-dose modified glucocerebrosidaseMISTRY, P. K; DAVIES, D; CORFIELD, A et al.Quarterly journal of medicine. 1992, Vol 83, Num 303, pp 541-546, issn 0033-5622Article

The Association Between Mutations in the Lysosomal Protein Glucocerebrosidase and ParkinsonismDEPAOLO, John; GOKER-ALPAN, Ozlem; SAMADDAR, Ted et al.Movement disorders. 2009, Vol 24, Num 11, pp 1571-1578, issn 0885-3185, 8 p.Article

Glucocerebrosidase Gene Mutations are Associated With Parkinson's Disease in Southern ItalyDE MARCO, Elvira V; ANNESI, Grazia; NICOLETTI, Giuseppe et al.Movement disorders. 2008, Vol 23, Num 3, pp 460-463, issn 0885-3185, 4 p.Article

Type I Gaucher disease with severe skeletal destruction, extraosseous extension, and monoclonal gammopathyKALOTERAKIS, A; CHOLONGITAS, E; PANTELIS, E et al.American journal of hematology. 2004, Vol 77, Num 4, pp 377-380, issn 0361-8609, 4 p.Article

Heterozygosity for a Mendelian disorder as a risk factor for complex diseaseSIDRANSKY, E.Clinical genetics. 2006, Vol 70, Num 4, pp 275-282, issn 0009-9163, 8 p.Article

Novel mutation, L371V, causing multigenerational Gaucher disease in a Lebanese familySHAMSEDDINE, A; TAHER, A; FAKHANI, S et al.American journal of medical genetics. 2004, Vol 125A, Num 3, pp 257-260, issn 0148-7299, 4 p.Article

Analysis of the glucocerebrosidase gene in Parkinson's diseaseSATO, Christine; MORGAN, Angharad; LANG, Anthony E et al.Movement disorders. 2004, Vol 20, Num 3, pp 367-370, issn 0885-3185, 4 p.Article

Response-Kriterien für die Enzymsubstitution bei Morbus Gaucher = Response criteria for enzyme replacement therapy in Morbus GaucherBERTHOLD, F; SIEVERTS, H; BENZ-BOHM, G et al.Monatsschrift für Kinderheilkunde. 1992, Vol 140, Num 10, pp 740-744, issn 0026-9298Article

Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's diseaseMURPHY, Karen E; GYSBERS, Amanda M; ABBOTT, Sarah K et al.Brain. 2014, Vol 137, pp 834-848, issn 0006-8950, 15 p., 3Article

Movement and mood disorder in two brothers with Gaucher diseaseRAJA, M; AZZONI, A; GIONA, F et al.Clinical genetics. 2007, Vol 72, Num 4, pp 357-361, issn 0009-9163, 5 p.Article

Acute neuronopathic gaucher disease complicated by fatal gastrointestinal bleedingHOFFMANN, B; SCHWAHN, B; KNOBBE, C. B et al.Neuropediatrics. 2006, Vol 37, Num 3, pp 163-165, issn 0174-304X, 3 p.Article

Gaucher disease : pathological mechanisms and modern managementJMOUDIAK, Marina; FUTERMAN, Anthony H.British journal of haematology. 2005, Vol 129, Num 2, pp 178-188, issn 0007-1048, 11 p.Article

Visual short-term memory deficits associated with GBA mutation and Parkinson's diseaseZOKAEI, Nahid; MCNEILL, Alisdair; HUSAIN, Masud et al.Brain. 2014, Vol 137, pp 2303-2311, issn 0006-8950, 9 p., 8Article

Gaucher Disease and Its Treatment OptionsBENNETT, Lunawati L; MOHAN, Devipriya.The Annals of pharmacotherapy. 2013, Vol 47, Num 9, pp 1182-1193, issn 1060-0280, 12 p.Article

Glucocerebrosidase Gene L444P Mutation is a Risk Factor for Parkinson's Disease in Chinese PopulationSUN, Qi-Ying; GUO, Ji-Feng; LEI WANG et al.Movement disorders. 2010, Vol 25, Num 8, pp 1005-1011, issn 0885-3185, 7 p.Article

Successful Pregnancy and Lactation Outcome in a Patient With Gaucher Disease Receiving Enzyme Replacement Therapy, and the Subsequent Distribution and Excretion of Imiglucerase in Human Breast MilkSEKIJIMA, Yoshiki; OHASHI, Toya; OHIRA, Satoshi et al.Clinical therapeutics. 2010, Vol 32, Num 12, pp 2048-2052, issn 0149-2918, 5 p.Article

Intrauterine onset of acute neuropathic type 2 Gaucher disease: Identification of a novel insertion sequenceFELDERHOFF-MUESER, Ursula; UHL, Johannes; PENZEL, Roland et al.American journal of medical genetics. 2004, Vol 128A, Num 2, pp 138-143, issn 0148-7299, 6 p.Article

GLUCOCEREBROSIDASE: RECONSTITUTION OF ACTIVITY FROM MACROMOLECULAR COMPONENTSMAE WAN HO; O'BRIEN JS; RADIN NS et al.1973; BIOCHEM. J.; G.B.; DA. 1973; VOL. 131; NO 1; PP. 173-176; BIBL. 10 REF.Serial Issue

Glucocerebrosidase is shaking up the synucleinopathiesSIEBERT, Marina; SIDRANSKY, Ellen; WESTBROEK, Wendy et al.Brain. 2014, Vol 137, pp 1304-1322, issn 0006-8950, 19 p., 5Article

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