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Results: 1-25 | 26-50 | 51-68
Results: 1-25/68
MANAGEMENT OF MULTIPLE-SCLEROSIS IN CHILDREN
Authors: HANEFELD F
Citation: F. Hanefeld, MANAGEMENT OF MULTIPLE-SCLEROSIS IN CHILDREN, European journal of neurology, 5, 1998, pp. 29-30
HYPERPHAGIA IN CHILDREN WITH CRANIOPHARYNGIOMA IS ASSOCIATED WITH HYPERLEPTINAEMIA AND A FAILURE IN THE DOWN-REGULATION OF APPETITE
Authors: ROTH C WILKEN B HANEFELD F SCHROTER W LEONHARDT U
Citation: C. Roth et al., HYPERPHAGIA IN CHILDREN WITH CRANIOPHARYNGIOMA IS ASSOCIATED WITH HYPERLEPTINAEMIA AND A FAILURE IN THE DOWN-REGULATION OF APPETITE, European journal of endocrinology, 138(1), 1998, pp. 89-91
IDENTICAL MITOCHONDRIAL-DNA IN MONOZYGOTIC TWINS WITH DISCORDANT ADRENOLEUKODYSTROPHY PHENOTYPE
Authors: WILICHOWSKI E OHLENBUSCH A KORENKE GC HUNNEMAN DH HANEFELD F
Citation: E. Wilichowski et al., IDENTICAL MITOCHONDRIAL-DNA IN MONOZYGOTIC TWINS WITH DISCORDANT ADRENOLEUKODYSTROPHY PHENOTYPE, Annals of neurology, 43(6), 1998, pp. 835-836
MOLECULAR CHARACTERIZATION OF 2 DELETION EVENTS INVOLVING ALU-SEQUENCES, ONE NOVEL BASE SUBSTITUTION AND 2 TENTATIVE HOTSPOT MUTATIONS IN THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) GENE IN 5 PATIENTS WITH LESCH-NYHAN-SYNDROME
Authors: TVRDIK T MARCUS S HOU SM FALT S NOORI P PODLUTSKAJA N HANEFELD F STROMME F LAMBERT B
Citation: T. Tvrdik et al., MOLECULAR CHARACTERIZATION OF 2 DELETION EVENTS INVOLVING ALU-SEQUENCES, ONE NOVEL BASE SUBSTITUTION AND 2 TENTATIVE HOTSPOT MUTATIONS IN THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) GENE IN 5 PATIENTS WITH LESCH-NYHAN-SYNDROME, Human genetics, 103(3), 1998, pp. 311-318
CHARACTERIZATION OF THE MITOCHONDRIAL GENOME IN CHILDHOOD MULTIPLE-SCLEROSIS - I - OPTIC NEURITIS AND LHON MUTATIONS
Authors: OHLENBUSCH A WILICHOWSKI E HANEFELD F
Citation: A. Ohlenbusch et al., CHARACTERIZATION OF THE MITOCHONDRIAL GENOME IN CHILDHOOD MULTIPLE-SCLEROSIS - I - OPTIC NEURITIS AND LHON MUTATIONS, Neuropediatrics, 29(4), 1998, pp. 175-179
CREATINE PROTECTS THE CENTRAL RESPIRATORY NETWORK OF MAMMALS UNDER ANOXIC CONDITIONS
Authors: WILKEN B RAMIREZ JM PROBST I RICHTER DW HANEFELD F
Citation: B. Wilken et al., CREATINE PROTECTS THE CENTRAL RESPIRATORY NETWORK OF MAMMALS UNDER ANOXIC CONDITIONS, Pediatric research, 43(1), 1998, pp. 8-14
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-V - DEFICIENCY OF DOLICHYL-P-GLC-MAN(9)GLCNAC(2)-PP-DOLICHYL GLUCOSYLTRANSFERASE
Authors: KORNER C KNAUER R HOLZBACH U HANEFELD F LEHLE L VONFIGURA K
Citation: C. Korner et al., CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-V - DEFICIENCY OF DOLICHYL-P-GLC-MAN(9)GLCNAC(2)-PP-DOLICHYL GLUCOSYLTRANSFERASE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(22), 1998, pp. 13200-13205
DOMAN-DELACATO APPROACH TO MOTOR AND DEVE LOPMENTAL DISORDERS - POSITION OF THE GESELLSCHAFT-FUR-NEUROPADIATRIE
Authors: GROSSSELBECK G HANEFELD F KARCH D RITZ A SCHLACK HG
Citation: G. Grossselbeck et al., DOMAN-DELACATO APPROACH TO MOTOR AND DEVE LOPMENTAL DISORDERS - POSITION OF THE GESELLSCHAFT-FUR-NEUROPADIATRIE, Monatsschrift fur Kinderheilkunde, 146(5), 1998, pp. 513-515
PYRUVATE-DEHYDROGENASE COMPLEX DEFICIENCY AND ALTERED RESPIRATORY-CHAIN FUNCTION IN A PATIENT WITH KEARNS-SAYRE MELAS OVERLAP SYNDROME AND A3243G MTDNA MUTATION/
Authors: WILICHOWSKI E KORENKE GC RUITENBEEK W DEMEIRLEIR L HAGENDORFF A JANSSEN AJM LISSENS W HANEFELD F
Citation: E. Wilichowski et al., PYRUVATE-DEHYDROGENASE COMPLEX DEFICIENCY AND ALTERED RESPIRATORY-CHAIN FUNCTION IN A PATIENT WITH KEARNS-SAYRE MELAS OVERLAP SYNDROME AND A3243G MTDNA MUTATION/, Journal of the neurological sciences, 157(2), 1998, pp. 206-213
LINKAGE ANALYSIS IN RETT-SYNDROME FAMILIES SUGGESTS THAT THERE MAY BEA CRITICAL REGION AT XQ28
Authors: WEBB T CLARKE A HANEFELD F PEREIRA JL ROSENBLOOM L WOODS CG
Citation: T. Webb et al., LINKAGE ANALYSIS IN RETT-SYNDROME FAMILIES SUGGESTS THAT THERE MAY BEA CRITICAL REGION AT XQ28, Journal of Medical Genetics, 35(12), 1998, pp. 997-1003
POTENTIAL PROGNOSTIC VALUE OF C-ERBB-2 EXPRESSION IN MEDULLOBLASTOMASIN VERY YOUNG-CHILDREN
Authors: HERMS JW BEHNKE J BERGMANN M CHRISTEN HJ KOLB R WILKENING M MARKAKIS E HANEFELD F KRETZSCHMAR HA
Citation: Jw. Herms et al., POTENTIAL PROGNOSTIC VALUE OF C-ERBB-2 EXPRESSION IN MEDULLOBLASTOMASIN VERY YOUNG-CHILDREN, Journal of pediatric hematology/oncology, 19(6), 1997, pp. 510-515
EARLY SEIZURE ONSET IN RETT-SYNDROME
Authors: SKJELDAL OH CHRISTEN HJ HAGNE I HANEFELD F HAGBERG B
Citation: Oh. Skjeldal et al., EARLY SEIZURE ONSET IN RETT-SYNDROME, European child & adolescent psychiatry, 6, 1997, pp. 40-41
LOCALIZED PROTON MAGNETIC-RESONANCE SPECTROSCOPY (MRS) OF THE BRAIN IN RETT-SYNDROME
Authors: BROCKMANN K HOLZBACH U KRUSE B CHRISTEN HJ POUWELS P FRAHM J HANEFELD F
Citation: K. Brockmann et al., LOCALIZED PROTON MAGNETIC-RESONANCE SPECTROSCOPY (MRS) OF THE BRAIN IN RETT-SYNDROME, European child & adolescent psychiatry, 6, 1997, pp. 67-67
INTRATHECAL IGA SYNTHESIS IN X-LINKED CEREBRAL ADRENOLEUKODYSTROPHY
Authors: KORENKE GC REIBER H HUNNEMAN DH HANEFELD F
Citation: Gc. Korenke et al., INTRATHECAL IGA SYNTHESIS IN X-LINKED CEREBRAL ADRENOLEUKODYSTROPHY, Journal of child neurology, 12(5), 1997, pp. 314-320
VARIABILITY OF ENDOCRINOLOGIC DYSFUNCTION IN 55 PATIENTS WITH X-LINKED ADRENOLEUKODYSTROPHY - CLINICAL, LABORATORY AND GENETIC FINDINGS
Authors: KORENKE GC ROTH C KRASEMANN E HUFNER M HUNNEMAN DH HANEFELD F
Citation: Gc. Korenke et al., VARIABILITY OF ENDOCRINOLOGIC DYSFUNCTION IN 55 PATIENTS WITH X-LINKED ADRENOLEUKODYSTROPHY - CLINICAL, LABORATORY AND GENETIC FINDINGS, European journal of endocrinology, 137(1), 1997, pp. 40-47
S-1 NUCLEASE HYBRID ANALYSIS OF MITOCHONDRIAL-DNA AMPLIFIED BY LONG-DISTANCE PCR - RAPID SCREENING FOR SMALL-SCALE REARRANGEMENTS
Authors: LUNDIN K WILICHOWSKI E ERNST BP HANEFELD F
Citation: K. Lundin et al., S-1 NUCLEASE HYBRID ANALYSIS OF MITOCHONDRIAL-DNA AMPLIFIED BY LONG-DISTANCE PCR - RAPID SCREENING FOR SMALL-SCALE REARRANGEMENTS, Nucleic acids research, 25(12), 1997, pp. 2535-2536
GC-MS DETERMINATION OF GUANIDINOACETATE IN URINE AND PLASMA
Authors: HUNNEMAN DH HANEFELD F
Citation: Dh. Hunneman et F. Hanefeld, GC-MS DETERMINATION OF GUANIDINOACETATE IN URINE AND PLASMA, Journal of inherited metabolic disease, 20(3), 1997, pp. 450-452
DECREASED PLATELET MEMBRANE ANISOTROPY IN PATIENTS WITH ADRENOLEUKODYSTROPHY TREATED WITH ERUCIC-ACID (22 1)-RICH TRIGLYCERIDES/
Authors: STOCKLER S OPPER C GREINACHER A HUNNEMAN DH KORENKE GC UNKRIG CJ HANEFELD F
Citation: S. Stockler et al., DECREASED PLATELET MEMBRANE ANISOTROPY IN PATIENTS WITH ADRENOLEUKODYSTROPHY TREATED WITH ERUCIC-ACID (22 1)-RICH TRIGLYCERIDES/, Journal of inherited metabolic disease, 20(1), 1997, pp. 54-58
PROGRESSION OF X-LINKED ADRENOLEUKODYSTROPHY UNDER INTERFERON-BETA THERAPY
Authors: KORENKE GC CHRISTEN HJ KRUSE B HUNNEMAN DH HANEFELD F
Citation: Gc. Korenke et al., PROGRESSION OF X-LINKED ADRENOLEUKODYSTROPHY UNDER INTERFERON-BETA THERAPY, Journal of inherited metabolic disease, 20(1), 1997, pp. 59-66
GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY - A NEWLY RECOGNIZED INBORN ERROR OF CREATINE BIOSYNTHESIS
Authors: STOCKLER S HANEFELD F
Citation: S. Stockler et F. Hanefeld, GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY - A NEWLY RECOGNIZED INBORN ERROR OF CREATINE BIOSYNTHESIS, Wiener Klinische Wochenschrift, 109(3), 1997, pp. 86-88
INTRACELLULAR SIGNAL PATHWAYS CONTROLLING RESPIRATORY NEURONS
Authors: RICHTER DW LALLEY PM PIERREFICHE O HAJI A BISCHOFF AM WILKEN B HANEFELD F
Citation: Dw. Richter et al., INTRACELLULAR SIGNAL PATHWAYS CONTROLLING RESPIRATORY NEURONS, Respiration physiology, 110(2-3), 1997, pp. 113-123
HYPOPARATHYROIDISM AND DEAFNESS ASSOCIATED WITH PLEIOPLASMIC LARGE-SCALE REARRANGEMENTS OF THE MITOCHONDRIAL-DNA - A CLINICAL AND MOLECULAR-GENETIC STUDY OF 4 CHILDREN WITH KEARNS-SAYRE-SYNDROME
Authors: WILICHOWSKI E GRUTERS A KRUSE K RATING D BEETZ R KORENKE GC ERNST BP CHRISTEN HJ HANEFELD F
Citation: E. Wilichowski et al., HYPOPARATHYROIDISM AND DEAFNESS ASSOCIATED WITH PLEIOPLASMIC LARGE-SCALE REARRANGEMENTS OF THE MITOCHONDRIAL-DNA - A CLINICAL AND MOLECULAR-GENETIC STUDY OF 4 CHILDREN WITH KEARNS-SAYRE-SYNDROME, Pediatric research, 41(2), 1997, pp. 193-200
LAUB,MICHAEL,C. - IN-MEMORIAM
Authors: RATING D BOENIGK HE HANEFELD F
Citation: D. Rating et al., LAUB,MICHAEL,C. - IN-MEMORIAM, Monatsschrift fur Kinderheilkunde, 145(8), 1997, pp. 870-870
DRUG AND DIETARY THERAPY IN MITOCHONDRIAL CYTOPATHIES OF CHILDHOOD
Authors: WILICHOWSKI E KORENKE GC CHRISTEN HJ WAGNER M RATING D HANEFELD F
Citation: E. Wilichowski et al., DRUG AND DIETARY THERAPY IN MITOCHONDRIAL CYTOPATHIES OF CHILDHOOD, Monatsschrift fur Kinderheilkunde, 145(1), 1997, pp. 5
GUANIDINO COMPOUNDS IN GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY,A NEW INBORN ERROR OF CREATINE SYNTHESIS
Authors: STOCKLER S MARESCAU B DEDEYN PP TRIJBELS JMF HANEFELD F
Citation: S. Stockler et al., GUANIDINO COMPOUNDS IN GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY,A NEW INBORN ERROR OF CREATINE SYNTHESIS, Metabolism, clinical and experimental, 46(10), 1997, pp. 1189-1193
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