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Results: 1-25 | 26-50 | 51-75 | 76-79
Results: 1-25/79
IDENTIFICATION OF A CANDIDATE MODIFYING GENE FOR SPINAL MUSCULAR-ATROPHY BY COMPARATIVE GENOMICS
Authors: SCHARF JM ENDRIZZI MG WETTER A HUANG S THOMPSON TG ZERRES K DIETRICH WF WIRTH B KUNKEL LM
Citation: Jm. Scharf et al., IDENTIFICATION OF A CANDIDATE MODIFYING GENE FOR SPINAL MUSCULAR-ATROPHY BY COMPARATIVE GENOMICS, Nature genetics, 20(1), 1998, pp. 83-86
AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE
Authors: ZERRES K RUDNIKSCHONEBORN S STEINKAMM C BECKER J MUCHER G
Citation: K. Zerres et al., AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE, Journal of molecular medicine, 76(5), 1998, pp. 303-309
KIDNEY GROWTH AND RENAL-FUNCTION IN UNILATERAL MULTICYSTIC DYSPLASTICKIDNEY-DISEASE
Authors: JOHN U RUDNIKSCHONEBORN S ZERRES K MISSELWITZ J
Citation: U. John et al., KIDNEY GROWTH AND RENAL-FUNCTION IN UNILATERAL MULTICYSTIC DYSPLASTICKIDNEY-DISEASE, Pediatric nephrology, 12(7), 1998, pp. 567-571
FINE MAPPING OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE LOCUS (PKHD1) AND THE GENES MUT, RDS, CSNK2-BETA, AND GSTA1 AT 6P21.1-P12
Authors: MUCHER G BECKER J KNAPP M BUTTNER R MOSER M RUDNIKSCHONEBORN S SOMLO S GERMINO G ONUCHIC L AVNER E GUAYWOODFORD L ZERRES K
Citation: G. Mucher et al., FINE MAPPING OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE LOCUS (PKHD1) AND THE GENES MUT, RDS, CSNK2-BETA, AND GSTA1 AT 6P21.1-P12, Genomics, 48(1), 1998, pp. 40-45
AXONAL NEUROPATHY AND PREDOMINANCE OF TYPE-II MYOFIBERS IN INFANTILE SPINAL MUSCULAR-ATROPHY
Authors: OMRAN H KETELSEN UP HEINEN F SAUER M RUDNIKSCHONEBORN S WIRTH B ZERRES K KRATZER W KORINTHENBERG R
Citation: H. Omran et al., AXONAL NEUROPATHY AND PREDOMINANCE OF TYPE-II MYOFIBERS IN INFANTILE SPINAL MUSCULAR-ATROPHY, Journal of child neurology, 13(7), 1998, pp. 327-331
CLINICAL-FEATURES OF UNILATERAL MULTICYSTIC RENAL DYSPLASIA IN CHILDREN
Authors: RUDNIKSCHONEBORN S JOHN U DEGET F EHRICH JHH MISSELWITZ J ZERRES K
Citation: S. Rudnikschoneborn et al., CLINICAL-FEATURES OF UNILATERAL MULTICYSTIC RENAL DYSPLASIA IN CHILDREN, European journal of pediatrics, 157(8), 1998, pp. 666-672
APOLIPOPROTEIN-E POLYMORPHISM INFLUENCES THE CEREBRAL METABOLIC PATTERN IN ALZHEIMERS-DISEASE
Authors: MIELKE R ZERRES K UHLHAAS S KESSLER J HEISS WD
Citation: R. Mielke et al., APOLIPOPROTEIN-E POLYMORPHISM INFLUENCES THE CEREBRAL METABOLIC PATTERN IN ALZHEIMERS-DISEASE, Neuroscience letters, 254(1), 1998, pp. 49-52
INCREASED RISK FOR ABNORMAL PLACENTATION IN WOMEN AFFECTED BY MYOTONIC-DYSTROPHY
Authors: RUDNIKSCHONEBORN S ROHRIG D ZERRES K
Citation: S. Rudnikschoneborn et al., INCREASED RISK FOR ABNORMAL PLACENTATION IN WOMEN AFFECTED BY MYOTONIC-DYSTROPHY, Journal of perinatal medicine, 26(3), 1998, pp. 192-195
COGNITIVE FUNCTION AND BEHAVIORAL-PROBLEMS IN CHILDREN AND ADOLESCENTS WITH SPINAL MUSCULAR-ATROPHY
Authors: VONGONTARD A ZERRES K LAUFERSWEILERPLASS C WENDLAND C RUDNIKSCHONEBORN S LEHMKUHL G
Citation: A. Vongontard et al., COGNITIVE FUNCTION AND BEHAVIORAL-PROBLEMS IN CHILDREN AND ADOLESCENTS WITH SPINAL MUSCULAR-ATROPHY, American journal of medical genetics, 81(6), 1998, pp. 550-550
PRENATAL-DIAGNOSIS OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE (ARPKD) - MOLECULAR-GENETICS, CLINICAL-EXPERIENCE, AND FETAL MORPHOLOGY
Authors: ZERRES K MUCHER G BECKER J STEINKAMM C RUDNIKSCHONEBORN S HEIKKILA P RAPOLA J SALONEN R GERMINO GG ONUCHIC L SOMLO S AVNER ED HARMAN LA STOCKWIN JM GUAYWOODFORD LM
Citation: K. Zerres et al., PRENATAL-DIAGNOSIS OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE (ARPKD) - MOLECULAR-GENETICS, CLINICAL-EXPERIENCE, AND FETAL MORPHOLOGY, American journal of medical genetics, 76(2), 1998, pp. 137-144
PHARMACOKINETICS OF SINGLE AND MULTIPLE-DOSE TROSPIUM CHLORIDE IN ELDERLY VOLUNTEERS USING A REPLICATIVE DESIGN
Authors: ZERRES K ZAIGLER M RIETBROCK S WEYHENMEYER R KRUMBIEGEL G FUHR U
Citation: K. Zerres et al., PHARMACOKINETICS OF SINGLE AND MULTIPLE-DOSE TROSPIUM CHLORIDE IN ELDERLY VOLUNTEERS USING A REPLICATIVE DESIGN, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 687-687
2 FORMS OF HEREDITARY SPASTIC CEREBRAL PARESIS WITH ONSET IN CHILDHOOD
Authors: HAVERKAMP F ZERRES K
Citation: F. Haverkamp et K. Zerres, 2 FORMS OF HEREDITARY SPASTIC CEREBRAL PARESIS WITH ONSET IN CHILDHOOD, Monatsschrift fur Kinderheilkunde, 146(6), 1998, pp. 574-579
ANALYSIS OF CREATINE-KINASE ACTIVITY IN 504 PATIENTS WITH PROXIMAL SPINAL MUSCULAR-ATROPHY TYPES I-III FROM THE POINT-OF-VIEW OF PROGRESSION AND SEVERITY
Authors: RUDNIKSCHONEBORN S LUTZENRATH S BORKOWSKA J KARWANSKA A HAUSMANOWAPETRUSEWICZ I ZERRES K
Citation: S. Rudnikschoneborn et al., ANALYSIS OF CREATINE-KINASE ACTIVITY IN 504 PATIENTS WITH PROXIMAL SPINAL MUSCULAR-ATROPHY TYPES I-III FROM THE POINT-OF-VIEW OF PROGRESSION AND SEVERITY, European neurology, 39(3), 1998, pp. 154-162
MISSENSE MUTATIONS IN EXON-6 OF THE SURVIVAL MOTOR-NEURON GENE IN PATIENTS WITH SPINAL MUSCULAR-ATROPHY (SMA)
Authors: HAHNEN E SCHONLING J RUDNIKSCHONEBORN S RASCHKE H ZERRES K WIRTH B
Citation: E. Hahnen et al., MISSENSE MUTATIONS IN EXON-6 OF THE SURVIVAL MOTOR-NEURON GENE IN PATIENTS WITH SPINAL MUSCULAR-ATROPHY (SMA), Human molecular genetics, 6(5), 1997, pp. 821-825
SPINAL MUSCULAR-ATROPHY - CLINICAL AND GENETIC CORRELATIONS
Authors: ZERRES K WIRTH B RUDNIKSCHONEBORN S
Citation: K. Zerres et al., SPINAL MUSCULAR-ATROPHY - CLINICAL AND GENETIC CORRELATIONS, Neuromuscular disorders, 7(3), 1997, pp. 202-207
ENHANCED APOPTOTIC CELL-DEATH OF RENAL EPITHELIAL-CELLS IN MICE LACKING TRANSCRIPTION FACTOR AP-2-BETA
Authors: MOSER M PSCHERER A ROTH C BECKER J MUCHER G ZERRES K DIXKENS C WEIS J GUAYWOODFORD L BUETTNER R FASSLER R
Citation: M. Moser et al., ENHANCED APOPTOTIC CELL-DEATH OF RENAL EPITHELIAL-CELLS IN MICE LACKING TRANSCRIPTION FACTOR AP-2-BETA, Genes & development, 11(15), 1997, pp. 1938-1948
AN INTEGRATED GENETIC AND PHYSICAL MAP OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE REGION
Authors: LENS XM ONUCHIC LF WU GQ HAYASHI T DAOUST M MOCHIZUKI T SANTARINA LB STOCKWIN JM MUCHER G BECKER J SWEENY WE AVNER ED GUAYWOODFORD L ZERRES K SOMLO S GERMINO GG
Citation: Xm. Lens et al., AN INTEGRATED GENETIC AND PHYSICAL MAP OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE REGION, Genomics, 41(3), 1997, pp. 463-466
CONGENITAL AXONAL NEUROPATHY CAUSED BY DELETIONS IN THE SPINAL MUSCULAR-ATROPHY REGION
Authors: KORINTHENBERG R SAUER M KETELSEN UP HANEMANN CO STOLL G GRAF M BABORIE A VOLK B WIRTH B RUDNIKSCHONEBORN S ZERRES K
Citation: R. Korinthenberg et al., CONGENITAL AXONAL NEUROPATHY CAUSED BY DELETIONS IN THE SPINAL MUSCULAR-ATROPHY REGION, Annals of neurology, 42(3), 1997, pp. 364-368
DIFFERENT ENTITIES OF PROXIMAL SPINAL MUSCULAR-ATROPHY WITHIN ONE FAMILY
Authors: WIRTH B TESSAROLO D HAHNEN E RUDNIKSCHONEBORN S RASCHKE H LIGUORI M GIACANELLI M ZERRES K
Citation: B. Wirth et al., DIFFERENT ENTITIES OF PROXIMAL SPINAL MUSCULAR-ATROPHY WITHIN ONE FAMILY, Human genetics, 100(5-6), 1997, pp. 676-680
SOMATIC AND PSYCHOMOTOR DEVELOPMENT IN CHILDREN WITH PENTA-X SYNDROME- 4 OWN OBSERVATIONS AND ANALYSIS OF PUBLISHED REPORTS
Authors: SCHULLER H ZERRES K RAFF R SCHWANITZ G
Citation: H. Schuller et al., SOMATIC AND PSYCHOMOTOR DEVELOPMENT IN CHILDREN WITH PENTA-X SYNDROME- 4 OWN OBSERVATIONS AND ANALYSIS OF PUBLISHED REPORTS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 278-278
A COLLABORATIVE STUDY ON THE NATURAL-HISTORY OF CHILDHOOD AND JUVENILE-ONSET PROXIMAL SPINAL MUSCULAR-ATROPHY (TYPE-II AND TYPE-III SMA) - 569 PATIENTS
Authors: ZERRES K RUDNIKSCHONEBORN S FORREST E LUSAKOWSKA A BORKOWSKA J HAUSMANOWAPETRUSEWICZ I
Citation: K. Zerres et al., A COLLABORATIVE STUDY ON THE NATURAL-HISTORY OF CHILDHOOD AND JUVENILE-ONSET PROXIMAL SPINAL MUSCULAR-ATROPHY (TYPE-II AND TYPE-III SMA) - 569 PATIENTS, Journal of the neurological sciences, 146(1), 1997, pp. 67-72
PROXIMAL AND DISTAL SPINAL MUSCULAR-ATROPHY IN ONE FAMILY - MOLECULAR-GENETIC STUDIES PROVIDE FURTHER EVIDENCE FOR THE NON-ALLELIC ORIGIN OF BOTH DISEASES
Authors: SPRANGER S RUDNIKSCHONEBORN S SPRANGER M SCHACHTELE M ZERRES K WIRTH B
Citation: S. Spranger et al., PROXIMAL AND DISTAL SPINAL MUSCULAR-ATROPHY IN ONE FAMILY - MOLECULAR-GENETIC STUDIES PROVIDE FURTHER EVIDENCE FOR THE NON-ALLELIC ORIGIN OF BOTH DISEASES, Journal of Medical Genetics, 34(4), 1997, pp. 340-342
AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE IN 115 CHILDREN - CLINICAL PRESENTATION, COURSE, AND INFLUENCE OF GENDER
Authors: ZERRES K RUDNIKSCHONEBOM S DEGET F
Citation: K. Zerres et al., AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE IN 115 CHILDREN - CLINICAL PRESENTATION, COURSE, AND INFLUENCE OF GENDER, Clinical pediatrics, 36(6), 1997, pp. 366-366
OBSTETRIC ASPECTS IN WOMEN WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, LIMB-GIRDLE MUSCULAR-DYSTROPHY, AND CONGENITAL MYOPATHIES
Authors: RUDNIKSCHONEBORN S GLAUNER B ROHRIG D ZERRES K
Citation: S. Rudnikschoneborn et al., OBSTETRIC ASPECTS IN WOMEN WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, LIMB-GIRDLE MUSCULAR-DYSTROPHY, AND CONGENITAL MYOPATHIES, Archives of neurology, 54(7), 1997, pp. 888-894
DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT OF INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE, AND IMPLICATIONS FOR GENETIC-COUNSELING
Authors: WIRTH B SCHMIDT T HAHNEN E RUDNIKSCHONEBORN S KRAWCZAK M MULLERMYHSOK B SCHONLING J ZERRES K
Citation: B. Wirth et al., DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT OF INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE, AND IMPLICATIONS FOR GENETIC-COUNSELING, American journal of human genetics, 61(5), 1997, pp. 1102-1111
Risultati: 1-25 | 26-50 | 51-75 | 76-79