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Results:
1-15
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Results: 15
Authors:
QUEISSERLUFT A
KIENINGERBAUM D
MENGER H
STOLZ G
SCHLAEFER K
MERZ E
Citation: A. Queisserluft et al., DOES MATERNAL OBESITY INCREASE THE RISK O F CONGENITAL-ANOMALIES - ANALYSIS OF 20,248 NEWBORN IN THE MAINZ BIRTH REGISTER, Ultraschall in der Medizin, 19(1), 1998, pp. 40-44
Authors:
MENGER H
LIN AE
TORIELLO HV
BERNERT G
SPRANGER JW
Citation: H. Menger et al., VITAMIN-K DEFICIENCY EMBRYOPATHY - A PHENOCOPY OF THE WARFARIN EMBRYOPATHY DUE TO A DISORDER OF EMBRYONIC VITAMIN-K METABOLISM, American journal of medical genetics, 72(2), 1997, pp. 129-134
Authors:
WILDHARDT G
WINTERPACHT A
HILBERT K
MENGER H
ZABEL B
Citation: G. Wildhardt et al., 2 DIFFERENT PAX3 GENE-MUTATIONS CAUSING WAARDENBURG SYNDROME TYPE-I, Molecular and cellular probes, 10(3), 1996, pp. 229-231
Authors:
MENGER H
MUNDLOS S
BECKER K
SPRANGER J
ZABEL B
Citation: H. Menger et al., AN UNKNOWN SPONDYLO-META-EPIPHYSEAL DYSPLASIA IN SIBS WITH EXTREME SHORT STATURE, American journal of medical genetics, 63(1), 1996, pp. 80-83
Authors:
HAENSCH CA
MENGER H
JORG J
Citation: Ca. Haensch et al., EVOKED-POTENTIALS AND MRT IN THE DIAGNOSI S OF THE SELDOM UNILATERAL SPINAL ARTERY SYNDROME, EEG-EMG, 26(2), 1995, pp. 95-99
Authors:
WINTERPACHT A
SCHWARZE U
MUNDLOS S
MENGER H
SPRANGER J
ZABEL B
Citation: A. Winterpacht et al., ALTERNATIVE SPLICING AS THE RESULT OF A TYPE-II PROCOLLAGEN GENE (COL2A1) MUTATION IN A PATIENT WITH KNIEST DYSPLASIA, Human molecular genetics, 3(10), 1994, pp. 1891-1893
Authors:
MENGER H
THALE J
OLBING B
ZIEMANN S
GULKER H
JORG J
Citation: H. Menger et al., EVALUATION OF TRANSESOPHAGEAL ECHOCARDIOG RAPHY IN CARDIOEMBOLIC STOKES, Nervenheilkunde, 13(4), 1994, pp. 186-191
Authors:
SPRANGER J
MENGER H
MUNDLOS S
WINTERPACHT A
ZABEL B
Citation: J. Spranger et al., KNIEST DYSPLASIA IS CAUSED BY DOMINANT COLLAGEN II (COL2A1) MUTATIONS- PARENTAL SOMATIC MOSAICISM MANIFESTING AS STICKLER PHENOTYPE AND MILD SPONDYLOEPIPHYSEAL DYSPLASIA, Pediatric radiology, 24(6), 1994, pp. 431-435
Authors:
MENGER H
NEUKATER W
KROLL S
JORG J
Citation: H. Menger et al., THE UVEOMENINGOENCEPHALITIC SYNDROME VOGT -KOYANAGI-HARADA, Nervenarzt, 65(8), 1994, pp. 553-556
Authors:
MENGER H
JORG J
BEDROSSIANPFINGSTEN J
Citation: H. Menger et al., NEUROLOGICAL COMPLICATIONS OF THE UNSPECI FIC BACTERIAL SPONDYLITIS, Nervenheilkunde, 12(8), 1993, pp. 421-430
Authors:
MENGER H
LINCKE HO
REMMERS J
Citation: H. Menger et al., COURSE OF MENINGEAL TUMOROUS SEED - ANALY SIS OF 85 PATIENTS, Aktuelle Neurologie, 20(6), 1993, pp. 196-202
Authors:
MENGER H
SCHREINER C
STEINER G
Citation: H. Menger et al., SUBACUTE PARAPARESIS THROUGH BILATERAL RE TROPERITONEAL HEMATOMAS DUETO ANTICOAGULANT-THERAPY, Aktuelle Neurologie, 20(6), 1993, pp. 218-220
Authors:
MENGER H
JOHANNSEN H
SCHWALEN S
RASTIN M
JORG J
CRAMER BM
Citation: H. Menger et al., CENTRAL PONTINE MYELINOLYSIS - PROGNOSTIC CHANGE IN A BRAIN-STEM DISEASE, Aktuelle Neurologie, 20(5), 1993, pp. 161-169
Authors:
MULLER FM
BARTH GM
MENGER H
SPRANGER J
Citation: Fm. Muller et al., CEREBRAL MALFORMATION, SEIZURES, HYPERTRICHOSIS, DISTINCT FACE, CLAW HANDS, AND OVERLAPPING FINGERS IN SIBS OF BOTH SEXES, American journal of medical genetics, 47(5), 1993, pp. 698-701
Authors:
MENGER H
PFINGSTEN H
HINTZE G
KOBBERLING J
JORG J
Citation: H. Menger et al., RARE DIFFERENTIAL-DIAGNOSIS OF WADDLING GAIT - OSTEOMALACIA DUE TO DEFICIENCY OF VITAMIN-D, Nervenarzt, 64(6), 1993, pp. 407-410
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