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Results: 1-25 | 26-36
Results: 1-25/36
V2 VASOPRESSIN RECEPTOR DYSFUNCTION IN NEPHROGENIC DIABETES-INSIPIDUSCAUSED BY DIFFERENT MOLECULAR MECHANISMS
Authors: SCHONEBERG T SCHULZ A BIEBERMANN H GRUTERS A GRIMM T HUBSCHMANN K FILLER G GUDERMANN T SCHULTZ G
Citation: T. Schoneberg et al., V2 VASOPRESSIN RECEPTOR DYSFUNCTION IN NEPHROGENIC DIABETES-INSIPIDUSCAUSED BY DIFFERENT MOLECULAR MECHANISMS, Human mutation, 12(3), 1998, pp. 196-205
A LINKAGE STUDY OF SPELLING DISORDER ON CHROMOSOME-1, CHROMOSOME-6, AND CHROMOSOME-15
Authors: SCHULTEKORNE G NOTHEN MM CICHON S GRIMM T MULLERMYHSOK B PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., A LINKAGE STUDY OF SPELLING DISORDER ON CHROMOSOME-1, CHROMOSOME-6, AND CHROMOSOME-15, American journal of medical genetics, 81(6), 1998, pp. 459-459
STATEMENT REGARDING ABORTION SUBSEQUENT TO PRENATAL DIAGNOSTIC STUDY
Authors: BACHMANN KD BERG D DUDENHAUSEN JW GRAUEL EL GRIMM T GRUNDEL J HEPP H HOLZGREVE W POHLANDT F SCHWINGER E VONSTOCKHAUSEN HB WOLFF G WOLFSLAST G WOLLERSHEIM RAU WOOPEN C WUERMELING HB
Citation: Kd. Bachmann et al., STATEMENT REGARDING ABORTION SUBSEQUENT TO PRENATAL DIAGNOSTIC STUDY, Monatsschrift fur Kinderheilkunde, 146(4), 1998, pp. 347-350
NO EVIDENCE FOR HETEROGENEITY IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY
Authors: KRESS W HALLIGERKELLER B GRIMM T PORSCHKE H ENGELHARDT A GOEBEL HH MULLERMYSOK B
Citation: W. Kress et al., NO EVIDENCE FOR HETEROGENEITY IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, Journal of Medical Genetics, 35(7), 1998, pp. 613-614
LINEAR AND WHORLED NEVOID HYPERMELANOSIS - CASE-REPORT AND REVIEW OF THE LITERATURE
Authors: HOFMANN U WAGNER N GRIMM T BROCKER EB HAMM H
Citation: U. Hofmann et al., LINEAR AND WHORLED NEVOID HYPERMELANOSIS - CASE-REPORT AND REVIEW OF THE LITERATURE, Hautarzt, 49(5), 1998, pp. 408-412
EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15
Authors: SCHULTEKORNE G GRIMM T NOTHEN MM MULLERMYHSOK B CICHON S VOGT IR PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15, American journal of human genetics, 63(1), 1998, pp. 279-282
OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN A NORTHERN GERMAN FAMILY LINKEDTO CHROMOSOME 14Q, AND PRESENTING CARNITINE DEFICIENCY
Authors: PORSCHKE H KRESS W REICHMANN H GOEBEL HH GRIMM T
Citation: H. Porschke et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN A NORTHERN GERMAN FAMILY LINKEDTO CHROMOSOME 14Q, AND PRESENTING CARNITINE DEFICIENCY, Neuromuscular disorders, 7, 1997, pp. 57-62
MISSENSE MUTATIONS AT ALA-10 IN THE FACTOR IX-PROPEPTIDE - A NOVEL MECHANISM FOR SEVERE BLEEDING DURING ORAL ANTICOAGULANT-THERAPY
Authors: OLDENBURG J QUENZEL M HARBRECHT U FREGIN A KRESS W GRIMM T HERTFELDER HJ SCHWAAB R BRACKMANN HH HANFLAND P
Citation: J. Oldenburg et al., MISSENSE MUTATIONS AT ALA-10 IN THE FACTOR IX-PROPEPTIDE - A NOVEL MECHANISM FOR SEVERE BLEEDING DURING ORAL ANTICOAGULANT-THERAPY, Thrombosis and haemostasis, 1997, pp. 720-720
EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15
Authors: SCHULTEKORNE G GRIMM T NOTHEN MM MULLERMYHSOK B PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15, American journal of medical genetics, 74(6), 1997, pp. 661-661
AN ANCESTRAL CORE HAPLOTYPE DEFINES THE CRITICAL REGION HARBORING THENORTH-CAROLINA MACULAR DYSTROPHY GENE (MCDR1)
Authors: SAUER CG SCHWORM HD ULBIG M BLANKENAGEL A ROHRSCHNEIDER K PAULEIKHOFF D GRIMM T WEBER BHF
Citation: Cg. Sauer et al., AN ANCESTRAL CORE HAPLOTYPE DEFINES THE CRITICAL REGION HARBORING THENORTH-CAROLINA MACULAR DYSTROPHY GENE (MCDR1), Journal of Medical Genetics, 34(12), 1997, pp. 961-966
MAPPING UNDETECTED MUTATIONS WITHIN A GENE - EVIDENCE FOR 2 PREFERENTIAL REGIONS IN THE DMD GENE
Authors: MULLERMYHSOK B HEILAND HJ MULLER CR MENG G GRIMM T OTT J
Citation: B. Mullermyhsok et al., MAPPING UNDETECTED MUTATIONS WITHIN A GENE - EVIDENCE FOR 2 PREFERENTIAL REGIONS IN THE DMD GENE, Human heredity, 47(2), 1997, pp. 61-65
ANALYSIS OF 21 STARGARDTS-DISEASE FAMILIES CONFIRMS A MAJOR LOCUS ON CHROMOSOME 1P WITH EVIDENCE FOR NON-ALLELIC HETEROGENEITY IN A MINORITY OF CASES
Authors: WEBER BHF SANDER S KOPP C WALKER D ECKSTEIN A WISSINGER B ZRENNER E GRIMM T
Citation: Bhf. Weber et al., ANALYSIS OF 21 STARGARDTS-DISEASE FAMILIES CONFIRMS A MAJOR LOCUS ON CHROMOSOME 1P WITH EVIDENCE FOR NON-ALLELIC HETEROGENEITY IN A MINORITY OF CASES, British journal of ophthalmology, 80(8), 1996, pp. 745-749
CHARACTERIZATION OF THE FACTOR-VIII DEFECT IN 147 PATIENTS WITH SPORADIC HEMOPHILIA-A - FAMILY STUDIES INDICATE A MUTATION TYPE-DEPENDENT SEX-RATIO OF MUTATION FREQUENCIES
Authors: BECKER J SCHWAAB R MOLLERTAUBE A SCHWAAB U SCHMIDT W BRACKMANN HH GRIMM T OLEK K OLDENBURG J
Citation: J. Becker et al., CHARACTERIZATION OF THE FACTOR-VIII DEFECT IN 147 PATIENTS WITH SPORADIC HEMOPHILIA-A - FAMILY STUDIES INDICATE A MUTATION TYPE-DEPENDENT SEX-RATIO OF MUTATION FREQUENCIES, American journal of human genetics, 58(4), 1996, pp. 657-670
BECKER,PETER,EMIL - A SHORT BIOGRAPHY ON THE OCCASION OF HIS 85TH BIRTHDAY
Authors: GRIMM T
Citation: T. Grimm, BECKER,PETER,EMIL - A SHORT BIOGRAPHY ON THE OCCASION OF HIS 85TH BIRTHDAY, Neuromuscular disorders, 5(3), 1995, pp. 243-247
THE TREATMENT OF GENETIC-DISEASES
Authors: GRIMM T
Citation: T. Grimm, THE TREATMENT OF GENETIC-DISEASES, Nervenheilkunde, 14(1), 1995, pp. 5-8
X-LINKED LYMPHOPROLIFERATIVE DISEASE (XLP ) - MOLECULAR-GENETIC STUDIES
Authors: SCHUSTER V GRIMM T KRESS W SEIDENSPINNER S BELOHRADSKY BH MULLER P KRETH HW
Citation: V. Schuster et al., X-LINKED LYMPHOPROLIFERATIVE DISEASE (XLP ) - MOLECULAR-GENETIC STUDIES, Klinische Padiatrie, 207(5), 1995, pp. 271-276
HOLT-ORAM SYNDROME IN COMBINATION WITH RE CIPROCAL TRANSLOCATION, PULMONARY HYPOPLASIA AND CARDIOMYOPATHY
Authors: KULLMANN F KOCH R FEICHTINGER W GIESEN H SCHMID M GRIMM T
Citation: F. Kullmann et al., HOLT-ORAM SYNDROME IN COMBINATION WITH RE CIPROCAL TRANSLOCATION, PULMONARY HYPOPLASIA AND CARDIOMYOPATHY, Klinische Padiatrie, 207(3), 1995, pp. 130-130
THE MYOTUBULAR MYOPATHIES - DIFFERENTIAL-DIAGNOSIS OF THE X-LINKED RECESSIVE, AUTOSOMAL-DOMINANT, AND AUTOSOMAL RECESSIVE FORMS AND PRESENTSTATE OF DNA STUDIES
Authors: WALLGRENPETTERSSON C CLARKE A SAMSON F FARDEAU M DUBOWITZ V MOSER H GRIMM T BAROHN RJ BARTH PG
Citation: C. Wallgrenpettersson et al., THE MYOTUBULAR MYOPATHIES - DIFFERENTIAL-DIAGNOSIS OF THE X-LINKED RECESSIVE, AUTOSOMAL-DOMINANT, AND AUTOSOMAL RECESSIVE FORMS AND PRESENTSTATE OF DNA STUDIES, Journal of Medical Genetics, 32(9), 1995, pp. 673-679
ESTIMATE OF SEVERE AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY(LGMD2C, LGMD2D) AMONG SPORADIC MUSCULAR-DYSTROPHY MALES - A STUDY OF415 FAMILIES
Authors: STEC I KRESS W MENG G MULLER B MULLER CR GRIMM T
Citation: I. Stec et al., ESTIMATE OF SEVERE AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY(LGMD2C, LGMD2D) AMONG SPORADIC MUSCULAR-DYSTROPHY MALES - A STUDY OF415 FAMILIES, Journal of Medical Genetics, 32(12), 1995, pp. 930-933
A MODIFIED SCREENING METHOD FOR PCDNA-1 EXPRESSION LIBRARIES WHICH ISAPPLICABLE TO BOTH SURFACE AND INTRACELLULAR ANTIGENS - CLONING OF A COLON-CARCINOMA ANTIGEN
Authors: GRIMM T JOHNSON JP
Citation: T. Grimm et Jp. Johnson, A MODIFIED SCREENING METHOD FOR PCDNA-1 EXPRESSION LIBRARIES WHICH ISAPPLICABLE TO BOTH SURFACE AND INTRACELLULAR ANTIGENS - CLONING OF A COLON-CARCINOMA ANTIGEN, Journal of immunological methods, 186(2), 1995, pp. 305-312
ECTOPIC EXPRESSION OF CARCINOEMBRYONIC ANTIGEN BY A MELANOMA CELL LEADS TO CHANGES IN THE TRANSCRIPTION OF 2 ADDITIONAL CELL-ADHESION MOLECULES
Authors: GRIMM T JOHNSON JP
Citation: T. Grimm et Jp. Johnson, ECTOPIC EXPRESSION OF CARCINOEMBRYONIC ANTIGEN BY A MELANOMA CELL LEADS TO CHANGES IN THE TRANSCRIPTION OF 2 ADDITIONAL CELL-ADHESION MOLECULES, Cancer research, 55(15), 1995, pp. 3254-3257
SEX-CHROMOSOME LOSS AND AGING - IN-SITU HYBRIDIZATION STUDIES ON HUMAN INTERPHASE NUCLEI
Authors: GUTTENBACH M KOSCHORZ B BERNTHALER U GRIMM T SCHMID M
Citation: M. Guttenbach et al., SEX-CHROMOSOME LOSS AND AGING - IN-SITU HYBRIDIZATION STUDIES ON HUMAN INTERPHASE NUCLEI, American journal of human genetics, 57(5), 1995, pp. 1143-1150
DISCORDANCE, IN A MALIGNANT HYPERTHERMIA PEDIGREE, BETWEEN IN-VITRO CONTRACTURE-TEST PHENOTYPES AND HAPLOTYPES FOR THE MHS1 REGION ON CHROMOSOME 19Q12-13.2, COMPRISING THE C1840T TRANSITION IN THE RYR1 GENE
Authors: DEUFEL T SUDBRAK R FEIST Y RUBSAM B DUCHESNE I SCHAFER KL ROEWER N GRIMM T LEHMANNHORN F HARTUNG EJ MULLER CR
Citation: T. Deufel et al., DISCORDANCE, IN A MALIGNANT HYPERTHERMIA PEDIGREE, BETWEEN IN-VITRO CONTRACTURE-TEST PHENOTYPES AND HAPLOTYPES FOR THE MHS1 REGION ON CHROMOSOME 19Q12-13.2, COMPRISING THE C1840T TRANSITION IN THE RYR1 GENE, American journal of human genetics, 56(6), 1995, pp. 1334-1342
PRECISE MAPPING OF THE BRAIN ALPHA(2)-ADRENERGIC RECEPTOR GENE WITHINCHROMOSOME 4P16
Authors: RIESS O THIES U SIEDLACZCK I POTISEK S GRAHAM R THEILMANN J GRIMM T EPPLEN JT HAYDEN MR
Citation: O. Riess et al., PRECISE MAPPING OF THE BRAIN ALPHA(2)-ADRENERGIC RECEPTOR GENE WITHINCHROMOSOME 4P16, Genomics, 19(2), 1994, pp. 298-302
THE HUMAN GENE FOR ALKAPTONURIA (AKU) MAPS TO CHROMOSOME 3Q
Authors: JANOCHA S WOLZ W SRSEN S SRSNOVA K MONTAGUTELLI X GUENET JL GRIMM T KRESS W MULLER CR
Citation: S. Janocha et al., THE HUMAN GENE FOR ALKAPTONURIA (AKU) MAPS TO CHROMOSOME 3Q, Genomics, 19(1), 1994, pp. 5-8
Risultati: 1-25 | 26-36