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