DETECTION OF G_M2-GANGHOSIDOSIS (TAY-SACHS AND SANDHOFF DISEASE) GENE CARRIERS BY SERUM HEXOSAMINIDASE ASSAY.MOLZER B; BERNHEIMER H.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 73; NO 1; PP. 163-169; BIBL. 22 REF.Article

LEUKOCYTE PPD-PEROXIDASE ACTIVITY WITH POLYUNSATURATED FATTY ACID HYDROPEROXIDES: NORMAL VALUES IN BATTEN'S DISEASESCHWERER B; BERNHEIMER H.1978; J. NEUROCHEM.; GBR; DA. 1978; VOL. 31; NO 2; PP. 457-460; BIBL. 30 REF.Article

BRAIN GANGLIOSIDES IN DRUG-INDUCED STATUS EPILEPTICUS = GANGLIOSIDES CEREBRAUX DANS L'EPILEPSIE INDUITE PAR LES DROGUESWINTER E; BERNHEIMER H.1975; J. NEUROCHEM.; G.B.; DA. 1975; VOL. 24; NO 3; PP. 591-592; BIBL. 9REF.Article

SANDHOFF DISEASE: GANGLIOSIDE G_M2 AND ASIALO G_M2 ACCUMULATION IN THE CEREBROSPINAL FLUID.BERNHEIMER H; MOLZER B; DEISENHAMMER E et al.1977; J. NEUROCHEM.; G.B.; DA. 1977; VOL. 29; NO 2; PP. 351-353; BIBL. 19 REF.Article

STRIATAL GANGLIOSIDE LEVELS IN THE RAT FOLLOWING KAINIC ACID LESIONS: COMPARISON WITH HUNTINGTON'S DISEASEHIGATSBERGER MR; SPERK G; BERNHEIMER H et al.1981; EXP. BRAIN RES.; ISSN 0014-4819; DEU; DA. 1981; VOL. 44; NO 1; PP. 93-96; BIBL. 38 REF.Article

SUSCEPTIBILITY OF MULTIPLY ANTIBIOTIC-RESISTANT PNEUMOCOCCI TO THE NEW BETA-LACTAM DRUGS AND ROSARAMICINLANDESMAN SH; COMMINGS M; GRUARIN A et al.1981; ANTIMICROB. AGENTS CHEMOTHER.; ISSN 0066-4804; USA; DA. 1981; VOL. 19; NO 4; PP. 675-677; BIBL. 4 REF.Article

REFSUM KRANKHEIT UND IHR VERLAUF BEI DIAETETISCHER BEHANDLUNG DURCH 21/2 JAHRE. KLINIK, BIOCHEMISCHE UND NEUROPATHOLOGISCHE DATEN = MALADIE DE REFSUM ET SON EVOLUTION SOUS TRAITEMENT DIETETIQUE DE 2 ANS 1/2. CLINIQUE, DONNEES BIOCHIMIQUES ET ANATOMOPATHOLOGIE DU SYSTEME NERVEUXLENZ H; SLUGA E; BERNHEIMER H et al.1979; NERVENARZT; DEU; DA. 1979; VOL. 50; NO 1; PP. 52-60; BIBL. 34 REF.Article

INFLUENCE OF CULTURAL CONDITIONS AND MUTATIONS ON THE COMPOSITION OF THE OUTER MEMBRANE PROTEINS OF ESCHERICHIA COLI.LUGTENBERG B; PETERS R; BERNHEIMER H et al.1976; MOLEC. GEN. GENET.; GERM.; DA. 1976; VOL. 147; NO 3; PP. 251-262; BIBL. 1 P.Article

Dynamics of IgG⁺, IgA⁺ and IgM⁺ plasma cells in the central nervous system of guinea pigs with chronic relapsing experimental allergic encephalomyelitisBERNHEIMER, H; LASSMANN, H; SUCHANEK, G et al.Neuropathology and applied neurobiology (Print). 1988, Vol 14, Num 2, pp 157-167, issn 0305-1846Article

Serum antibodies against glycosphingolipids on chronic relapsing experimental allergic encephalomyelitis. Demonstration by ELISA and relation to serum in vivo demyelinating activitySCHWERER, B; KITZ, K; LASSMANN, H et al.Journal of neuroimmunology. 1984, Vol 7, Num 2-3, pp 107-119, issn 0165-5728Article

Distinct immunoglobulin class and immunoglobulin G subclass patterns against ganglioside GQ1b in Miller Fisher syndrome following different types of infectionSCHWERER, B; NEISSER, A; BERNHEIMER, H et al.Infection and immunity. 1999, Vol 67, Num 5, pp 2414-2420, issn 0019-9567Article

Simultaneous detection of the two most frequent metachromatic leukodystrophy mutationsBERGER, J; MOLZER, B; GIESELMANN, V et al.Human genetics. 1993, Vol 92, Num 4, pp 421-423, issn 0340-6717Article

ELISA for determination in the nanogram range: assay in cerebrospinal fluid and comparison with radial immunodiffusionSCHWERER, B; BACH, M; BERNHEIMER, H et al.Clinica chimica acta. 1987, Vol 163, Num 3, pp 237-244, issn 0009-8981Article

Ganglioside G_M1, a molecular target for immunological and toxic attacks: similarity of neuropathological lesions induced by ganglioside-antiserum and cholera toxinSCHWERER, B; LASSMANN, H; KITZ, K et al.Acta neuropathologica. 1986, Vol 72, Num 1, pp 55-61, issn 0001-6322Article

KLINISCH-BIOCHEMISCHE VERLAUFSUNTERSUCHUNGEN BEI HEREDOPATHIA ATACTICA POLYNEURITIFORMIS (MORBUS REFSUM) = SURVEILLANCE CLINIQUE ET BIOCHIMIQUE DE LA MALADIE DE REFSUMBAROLIN GS; HODKEWITSCH E; HOEFINGER E et al.1979; FORTSCHR. NEUROL. PSYCHIATR. GRENZGEL.; DEU; DA. 1979; VOL. 47; NO 2; PP. 53-66; ABS. ENG; BIBL. 1 P.Article

Unusual orthochromatic leukodystrophy with epitheloid cells (Norman-Gullotta) : increase of very long chain fatty acids in brain discloses a peroxisomal disorderMOLZER, B; GULLOTTA, F; HARZER, K et al.Acta neuropathologica. 1993, Vol 86, Num 2, pp 187-189, issn 0001-6322Article

Refsum's disease in an Arabian familyFERTL, E; FÖLDY, D; VASS, K et al.Journal of neurology, neurosurgery and psychiatry. 2001, Vol 70, Num 4, pp 564-565, issn 0022-3050Article

Serum IgA and IgM antibodies against Mycobacterium leprae-derived phenolic glycolipid-I : a comparative study in Leprosy patients and their contactsCHUJOR, C. S. N; BERNHEIMER, H; LEVIS, W. R et al.International journal of leprosy and other mycobacterial diseases. 1991, Vol 59, Num 3, pp 441-449, issn 0148-916XArticle

Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variantsMOLZER, B; KORSCHINSKY, M; BERNHEIMER, H et al.Clinica chimica acta. 1986, Vol 161, Num 1, pp 81-90, issn 0009-8981Article

Specific inhibition of mRNA accumulation for lymphokines in human T cell line Jurkat by mycobacterial lipoarabinommanan antigenCHUJOR, C. S. N; KUHN, B; SCHWERER, B et al.Clinical and experimental immunology (Print). 1992, Vol 87, Num 3, pp 398-403, issn 0009-9104Article

Adrenoleukodystrophy in an adult female. A clinical, morphological, and neurochemical studySCHOLTE, W; MOLZER, B; PEIFFER, J et al.Journal of neurology. 1987, Vol 235, Num 1, pp 1-9, issn 0340-5354Article

Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies : Female adrenoleukodystrophy-like disease and late-onset Krabbe diseaseGULLOTTA, F; HUGHES, J. L; WITTKOWSKI, W et al.Neuropediatrics. 1996, Vol 27, Num 1, pp 37-41, issn 0174-304XArticle

IgA antibodies against phenolic glycolipid I from Mycobacterium leprae in serum of leprosy patients and contacts: subclass distribution and relation to disease activitySCHWERER, B; CHUJOR, C. S. N; BERNHEIMER, H et al.Clinical immunology and immunopathology (Print). 1989, Vol 53, Num 2, pp 202-211, issn 0090-1229, . 1Article

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob diseaseZERR, I; POCCHIARI, M; LADOGANA, A et al.Neurology. 2000, Vol 55, Num 6, pp 811-815, issn 0028-3878Article