Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("SCHWARZ, M. J")

Publication Year[py]

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

Discipline (document) [di]

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

Author Country

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

Results 1 to 17 of 17

  • Page / 1
Export

Selection :

  • and

Borna disease virus in human brains with a rare form of hippocampal degeneration but not in brains of patients with common neuropsychiatric disordersCZYGAN, M; HALLENSLEBEN, W; SCHWARZ, M. J et al.The Journal of infectious diseases. 1999, Vol 180, Num 5, pp 1695-1699, issn 0022-1899Article

Increase in expression of adhesion molecule receptors on T helper cells during antipsychotic treatment and relationship to blood-brain barrier permeability in schizophreniaMÜLLER, N; RIEDEL, M; HADJAMU, M et al.The American journal of psychiatry. 1999, Vol 156, Num 4, pp 634-636, issn 0002-953XArticle

Blood-cerebrospinal fluid barrier impairment as indicator for an immune process in schizophreniaSCHWARZ, M. J; ACKENHEIL, M; RIEDEL, M et al.Neuroscience letters. 1998, Vol 253, Num 3, pp 201-203, issn 0304-3940Article

Antibodies to heat shock proteins in schizophrenic patients : Implications for the mechanism of the diseaseSCHWARZ, M. J; RIEDEL, M; GRUBER, R et al.The American journal of psychiatry. 1999, Vol 156, Num 7, pp 1103-1104, issn 0002-953XArticle

Lyme disease presenting as Tourette's syndromeRIEDEL, M; STRAUBE, A; SCHWARZ, M. J et al.Lancet (British edition). 1998, Vol 351, Num 9100, pp 418-419, issn 0140-6736Article

Partial deletion 8q without Langer-Giedion syndrome: a recognisable syndromeFENNELL, S. J; BENSON, J. W. T; KINDLEY, A. D et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 167-171, issn 0022-2593, 5 p.Article

The th2-hypothesis of schizophrenia: a strategy to identify a subgroup of schizophrenia caused by immune mechanismsSCHWARZ, M. J; MÜLLER, N; RIEDEL, M et al.Medical hypotheses. 2001, Vol 56, Num 4, pp 483-486, issn 0306-9877Article

Discriminant power of combined cerebrospinal fluid T protein and of the soluble interleukin-6 receptor complex in the diagnosis of alzheimer's diseaseHAMPEL, H; TEIPEL, S. J; DUKOFF, R et al.Brain research. 1999, Vol 823, Num 1-2, pp 104-112, issn 0006-8993Article

Cerebrospinal fluid tau protein shows a better discrimination in young old (<70 years) than in old old patients with Alzheimer's disease compared with controlsBÜRGER, K; PADBERG, F; MÖLLER, H.-J et al.Neuroscience letters. 1999, Vol 277, Num 1, pp 21-24, issn 0304-3940Article

Active cascade testing for carriers of cystic fibrosis gene. CommentarySUPER, M; SCHWARZ, M. J; MALONE, G et al.BMJ. British medical journal (International ed.). 1994, Vol 308, Num 6942, pp 1462-1468, issn 0959-8146Article

Development, multiplexing, and application of ARMS tests for common mutations in the CFTR geneFERRIE, R. M; SCHWARZ, M. J; ROBERTSON, N. H et al.American journal of human genetics. 1992, Vol 51, Num 2, pp 251-262, issn 0002-9297Article

The cyclooxygenase-2 inhibitor celecoxib has therapeutic effects in major depression : results of a double-blind, randomized, placebo controlled, add-on pilot study to reboxetineMÜLLER, N; SCHWARZ, M. J; MÖLLER, H.-J et al.Molecular psychiatry. 2006, Vol 11, Num 7, pp 680-684, issn 1359-4184, 5 p.Article

Relationship of substance P, 5-hydroxyindole acetic acid and tryptophan in serum of fibromyalgia patientsSCHWARZ, M. J; SPÄTH, M; MÜLLER-BARDORFF, H et al.Neuroscience letters. 1999, Vol 259, Num 3, pp 196-198, issn 0304-3940Article

Interleukin-6 and the soluble IL-6 receptor are decreased in cerebrospinal fluid of geriatric patients with major depression : no alteration of soluble gp130STÜBNER, S; SCHÖN, T; SUNDERLAND, T et al.Neuroscience letters. 1999, Vol 259, Num 3, pp 145-148, issn 0304-3940Article

Interleukin-6 is not altered in cerebrospinal fluid of first-degree relatives and patients with Alzheimer's diseaseHAMPEL, H; SCHOEN, D; BUCH, K et al.Neuroscience letters. 1997, Vol 228, Num 3, pp 143-146, issn 0304-3940Article

Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk and meconium illeusHAMOSH, A; KING, T. M; MACEK, M. JR et al.American journal of human genetics. 1992, Vol 51, Num 2, pp 245-250, issn 0002-9297Article

Mutations of the cystic fibrosis gene locus within the population of the Northwest of EnglandSUPER, M; SCHWARZ, M. J.European journal of pediatrics. 1992, Vol 151, Num 2, pp 108-111, issn 0340-6199Article

  • Page / 1