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Authors: EVERS S BAUER B GROTEMEYER KH KURLEMANN G HUSSTEDT IW
Citation: S. Evers et al., EVENT-RELATED POTENTIALS (P300) IN PRIMARY HEADACHE IN CHILDHOOD AND ADOLESCENCE, Journal of child neurology, 13(7), 1998, pp. 322-326

Authors: STOGBAUER F YOUNG P KUHLENBAUMER G MEULEMAN J TIMMERMAN V VANBROECKHOVEN C KURLEMANN G RINGELSTEIN EB
Citation: F. Stogbauer et al., HEREDITARY NEURALGIC AMYOTROPHY (HNA) - C LINICAL FINDINGS AND MOLECULAR-GENETICS, Fortschritte der Neurologie, Psychiatrie, 66(1), 1998, pp. 10-14

Authors: JAKSCH M KLOPSTOCK T KURLEMANN G DORNER M HOFMANN S KLEINLE S HEGEMANN S WEISSERT M MULLERHOCKER J PONGRATZ D GERBITZ KD
Citation: M. Jaksch et al., PROGRESSIVE MYOCLONUS EPILEPSY AND MITOCHONDRIAL MYOPATHY ASSOCIATED WITH MUTATIONS IN THE TRNA(SER(UCN)) GENE, Annals of neurology, 44(4), 1998, pp. 635-640

Authors: WOESLER B KUWERT T KURLEMANN G MORGENROTH C PROBSTCOUSIN S LERCH H GULLOTTA F WASSMANN H SCHOBER O
Citation: B. Woesler et al., HIGH AMINO-ACID-UPTAKE IN A LOW-GRADE DESMOPLASTIC INFANTILE GANGLIOGLIOMA IN A 14-YEAR-OLD PATIENT, Neurosurgical review, 21(1), 1998, pp. 31-35

Authors: STOGBAUER F YOUNG P WIEBUSCH H TIMMERMAN V KUHLENBAUMER G NELIS E RINGELSTEIN EB KURLEMANN G ASSMANN G VANBROECKHOVEN C FUNKE H
Citation: F. Stogbauer et al., ABSENCE OF MUTATIONS IN PERIPHERAL MYELIN PROTEIN-22, MYELIN PROTEIN ZERO, AND CONNEXIN-32 IN AUTOSOMAL RECESSIVE DEJERINE-SOTTAS-SYNDROME, Neuroscience letters, 240(1), 1998, pp. 1-4

Authors: MOLENKAMP G RIEMANN B KUWERT T STRATER R KURLEMANN G SCHOBER O JURGENS H WOLFF JEA
Citation: G. Molenkamp et al., MONITORING TUMOR-ACTIVITY IN LOW-GRADE GLIOMA OF CHILDHOOD, Klinische Padiatrie, 210(4), 1998, pp. 239-242

Authors: FREUND A KURLEMANN G SCHUIERER G ULLRICH K
Citation: A. Freund et al., TUBERCULOUS MENINGITIS IN A 13-MONTH OLD BOY - A CASE-REPORT, Klinische Padiatrie, 210(3), 1998, pp. 132-135

Authors: BICK U SPRINZ A WEGLAGE J RENER BC KURLEMANN G SCHUIERER G
Citation: U. Bick et al., POSSIBLE LONG-TERM EFFECTS OF FEBRILE CONVULSIONS IN CHILDHOOD - A MRI VOLUMETRY STUDY OF THE HIPPOCAMPUS, Radiology, 209P, 1998, pp. 824-824

Authors: KURLEMANN G SCHUIERER G
Citation: G. Kurlemann et G. Schuierer, ASH-LEAF SPOTS IN TUBEROUS SCLEROSIS, The New England journal of medicine, 338(26), 1998, pp. 1887-1887

Authors: FREUND A ZASS R KURLEMANN G SCHUIERER G ULLRICH K
Citation: A. Freund et al., BILATERAL EDEMA OF THE BASAL GANGLIA IN AN ECHOVIRUS TYPE-21 INFECTION - COMPLETE CLINICAL AND RADIOLOGICAL NORMALIZATION, Developmental Medicine and Child Neurology, 40(6), 1998, pp. 421-424

Authors: DEBUS O KOCH HG KURLEMANN G STRATER R VIELHABER H WEBER P NOWAKGOTTL U
Citation: O. Debus et al., FACTOR-V-LEIDEN AND GENETIC-DEFECTS OF THROMBOPHILIA IN CHILDHOOD PORENCEPHALY, Archives of Disease in Childhood, 78(2), 1998, pp. 121-124

Authors: DALDRUP HE SCHUIERER G LINK TM MOELLER H BICK U KURLEMANN G PETERS PE
Citation: He. Daldrup et al., EVALUATION OF MYELINATION AND MYELINATION DISORDERS WITH TURBO INVERSION-RECOVERY MAGNETIC-RESONANCE-IMAGING, European radiology, 7(9), 1997, pp. 1478-1484

Authors: KURLEMANN G BENNER T BRAMSWIG HJ
Citation: G. Kurlemann et al., ADULT HEIGHT AND TARGET HEIGHT IN 111 BOYS AND 98 GIRLS TREATED FOR EPILEPSY DURING CHILDHOOD, Journal of child neurology, 12(8), 1997, pp. 513-515

Authors: STOGBAUER F YOUNG P TIMMERMAN V SPOELDERS P RINGELSTEIN EB VANBROECKHOVEN C KURLEMANN G
Citation: F. Stogbauer et al., REFINEMENT OF THE HEREDITARY NEURALGIC AMYOTROPHY (HNA) LOCUS TO CHROMOSOME 17Q24-Q25, Human genetics, 99(5), 1997, pp. 685-687

Authors: VIELHABER H DEBUS O FINDEISEN M KOCH HG KURLEMANN G STRATER R NOWAKGOTTL U
Citation: H. Vielhaber et al., FACTOR-V-LEIDEN, FURTHER INHIBITORS OF THE PROTEIN-C ANTICOAGULANT PATHWAY AND LIPOPROTEIN (A) IN CHILDHOOD STROKE, Thrombosis and haemostasis, 1997, pp. 409-409

Authors: FINDEISEN M DEBUS O KURLEMANN G POLLMANN H VIELHABER H NOWAKGOTTL U
Citation: M. Findeisen et al., APOLIPOPROTEIN (A) - ITS ROLE IN CHILDHOOD THROMBOEMBOLISM, Thrombosis and haemostasis, 1997, pp. 2967-2967

Authors: KURLEMANN G DEUFEL T SCHUIERER G
Citation: G. Kurlemann et al., PYRIDOXINE - RESPONSIVE WEST-SYNDROME AND GAMMA-AMINOBUTYRIC-ACID, European journal of pediatrics, 156(2), 1997, pp. 158-159

Authors: STRATER R KURLEMANN G SCHUIERER G LASJAUNIAS P PALM DG
Citation: R. Strater et al., ARTERIOVENOUS MALFORMATION OF THE CERVICA L-SPINE, Klinische Padiatrie, 209(2), 1997, pp. 84-87

Authors: RUNDE J EBBECKE H KURLEMANN G FROSCH M SCHUIERER G
Citation: J. Runde et al., SINUSHISTIOCYTOSIS WITH MASSIVE LYMPHADEN OPATHY COMPLICATED BY AN OBSTRUCTION OF THE VENA-CAVA-SUPERIOR AND INFERIOR, Klinische Padiatrie, 209(1), 1997, pp. 39-42

Authors: HEIM P CLAUSSEN M HOFFMANN B CONZELMANN E GARTNER J HARZER K HUNNEMAN DH KOHLER W KURLEMANN G KOHLSCHUTTER A
Citation: P. Heim et al., LEUKODYSTROPHY INCIDENCE IN GERMANY, American journal of medical genetics, 71(4), 1997, pp. 475-478

Authors: RAMBECK B KURLEMANN G STODIECK SRG MAY TW JURGENS U
Citation: B. Rambeck et al., CONCENTRATIONS OF LAMOTRIGINE IN A MOTHER ON LAMOTRIGINE TREATMENT AND HER NEWBORN CHILD, European Journal of Clinical Pharmacology, 51(6), 1997, pp. 481-484

Authors: WEGLAGE J DEMSKY A PIETSCH M KURLEMANN G
Citation: J. Weglage et al., NEUROPSYCHOLOGICAL, INTELLECTUAL, AND BEHAVIORAL FINDINGS IN PATIENTSWITH CENTROTEMPORAL SPIKES WITH AND WITHOUT SEIZURES, Developmental Medicine and Child Neurology, 39(10), 1997, pp. 646-651

Authors: WEBER P KURLEMANN G LUNECKE C TONDERA A
Citation: P. Weber et al., SOLAR RETINOPATHY, A RARE CAUSE OF ACUTE LOSS OF VISION, Deutsche Medizinische Wochenschrift, 121(24), 1996, pp. 793-796

Authors: KURLEMANN G DEBUS O SCHUIERER G
Citation: G. Kurlemann et al., DEXTROMETHORPHAN IN MOLYBDENUM COFACTOR DEFICIENCY, European journal of pediatrics, 155(5), 1996, pp. 422-423

Authors: STRATER R KURLEMANN G SCHUIERER G HARZER K GULOTTA F PALM DG
Citation: R. Strater et al., KRABBES DISEASE - UNIFORMITY AND VARIABIL ITY OF THE SYMPTOMS, Aktuelle Neurologie, 23(4), 1996, pp. 151-154
Risultati: 1-25 | 26-48