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Authors: VANBELZEN MJ HIEL JAP WEEMAES CMR GABREELS FJM VANENGELEN BGM SMEETS DFCM VANDENHEUVEL LPWJ
Citation: Mj. Vanbelzen et al., A DOUBLE MISSENSE MUTATION IN THE ATM GENE OF A DUTCH FAMILY WITH ATAXIA-TELANGIECTASIA, Human genetics, 102(2), 1998, pp. 187-191

Authors: TERLAAK HJ LEYTEN QH GABREELS FJM KUPPEN H RENIER WO SENGERS RCA
Citation: Hj. Terlaak et al., LAMININ-ALPHA(2) (MEROSIN), BETA-DYSTROGLYCAN, ALPHA-SARCOGLYCAN (ADHALIN), AND DYSTROPHIN EXPRESSION IN CONGENITAL MUSCULAR-DYSTROPHIES - AN IMMUNOHISTOCHEMICAL STUDY, Clinical neurology and neurosurgery, 100(1), 1998, pp. 5-10

Authors: HIEL JAP VERRIPS A KEYSER A JANSEN TLTA WESSELING P DECOO R GABREELS FJM
Citation: Jap. Hiel et al., ILEUS IN MITOCHONDRIAL ENCEPHALOMYOPATHY, LACTIC-ACIDOSIS AND STROKE-LIKE EPISODES, Netherlands journal of medicine, 53(1), 1998, pp. 27-31

Authors: GERRITS GPJM KAMPHUIS S MONNENS LAH TRIJBELS LAH SCHRODER CH KOSTER A GABREELS FJM
Citation: Gpjm. Gerrits et al., CEREBROSPINAL-FLUID LEVELS OF AMINO-ACIDS IN INFANTS AND YOUNG-CHILDREN WITH CHRONIC-RENAL-FAILURE, Neuropediatrics, 29(1), 1998, pp. 35-39

Authors: VANENGELEN BGM BENDERS AAGM WEVERS RA GABREELS FJM RENIER WO VEERKAMP JH
Citation: Bgm. Vanengelen et al., INTRAVENOUS IMMUNOGLOBULIN PREPARATION INCREASES MYOPLASMIC CALCIUM-CONCENTRATION BY ACTIVATING THE DIHYDROPYRIDINE-RYANODINE RECEPTOR COMPLEX, Journal of the neurological sciences, 156(1), 1998, pp. 35-40

Authors: BRAUTIGAM C WEVERS RA JANSEN RJT SMEITINK JAM DERIJKVANANDEL JF GABREELS FJM HOFFMANN GF
Citation: C. Brautigam et al., BIOCHEMICAL HALLMARKS OF TYROSINE-HYDROXYLASE DEFICIENCY, Clinical chemistry, 44(9), 1998, pp. 1897-1904

Authors: WILLEMSEN MAAP VANOORT AM TERLAAK HJ SENGERS RCA GABREELS FJM
Citation: Maap. Willemsen et al., MULTICORE MYOPATHY WITH RESTRICTIVE CARDIOMYOPATHY, Acta paediatrica, 86(11), 1997, pp. 1271-1274

Authors: VERRIPS A STEENBERGENSPANJERS GCH LUYTEN JAFM WEVERS RA WOKKE JHJ GABREELS FJM WOLTHERS BG VANDENHEUVEL LPWJ
Citation: A. Verrips et al., EXON SKIPPING IN THE STEROL 27-HYDROXYLASE GENE LEADS TO CEREBROTENDINOUS XANTHOMATOSIS, Human genetics, 100(2), 1997, pp. 284-286

Authors: STOLWIJK AM JONGBLOET PH ZIELHUIS GA GABREELS FJM
Citation: Am. Stolwijk et al., SEASONAL-VARIATION IN THE PREVALENCE OF DOWN-SYNDROME AT BIRTH - A REVIEW, Journal of epidemiology and community health, 51(4), 1997, pp. 350-353

Authors: BLATTER BM LAFEBER AB PETERS PWJ ROELEVELD N VERBEEK ALM GABREELS FJM
Citation: Bm. Blatter et al., HETEROGENEITY OF SPINA-BIFIDA, Teratology, 55(4), 1997, pp. 224-230

Authors: GIBSON KM CHRISTENSEN E JAKOBS C FOWLER B CLARE MA HAMMERSEN G RAAB K KOBORI J MOOSA A VOLLMER B ROSSIER E IAFOLLA AK MATERN D BROUWER OF FINELSTEIN J AKSU F WEBER HP BAKKEREN JAJM GABREELS FJM BLUESTONE D BARRON TF BEAUVAIS P RABIER D SANTOS C UMANSKY R LEHNERT W
Citation: Km. Gibson et al., THE CLINICAL PHENOTYPE OF SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY (4-HYDROXYBUTYRIC ACIDURIA) - CASE-REPORTS OF 23 NEW PATIENTS, Pediatrics, 99(4), 1997, pp. 567-574

Authors: VANDERKNAAP MS BARTH PG GABREELS FJM FRANZONI E BEGEER JH STROINK H ROTTEVEEL JJ VALK J
Citation: Ms. Vanderknaap et al., A NEW LEUKOENCEPHALOPATHY WITH VANISHING WHITE-MATTER, Neurology, 48(4), 1997, pp. 845-855

Authors: VANENGELEN BGM VANALFEN N GABREELS FJM
Citation: Bgm. Vanengelen et al., NATURAL-HISTORY OF HEREDITARY NEURALGIC AMYOTROPHY (HNA), Neurology, 48(3), 1997, pp. 9004-9004

Authors: MOURMANS J WENDEL U BENTLAGE HACM TRIJBELS JMF SMEITINK JAM DECOO IFM GABREELS FJM SENGERS RCA RUITENBEEK W
Citation: J. Mourmans et al., CLINICAL HETEROGENEITY IN RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY INCHILDHOOD, Journal of the neurological sciences, 149(1), 1997, pp. 111-117

Authors: KERSEMAEKERS WM ROELEVELD N ZIELHUIS GA GABREELS FJM
Citation: Wm. Kersemaekers et al., NEURODEVELOPMENT IN OFFSPRING OF HAIRDRESSERS, Developmental Medicine and Child Neurology, 39(6), 1997, pp. 358-362

Authors: BLATTER BM ROELEVELD N ZIELHUIS GA GABREELS FJM VERBEEK ALM
Citation: Bm. Blatter et al., MATERNAL OCCUPATIONAL EXPOSURE DURING PREGNANCY AND THE RISK OF SPINA-BIFIDA, Occupational and environmental medicine, 53(2), 1996, pp. 80-86

Authors: BLATTER BM ROELEVELD N ZIELHUIS GA MULLAART RA GABREELS FJM
Citation: Bm. Blatter et al., SPINA-BIFIDA AND PARENTAL OCCUPATION, Epidemiology, 7(2), 1996, pp. 188-193

Authors: VERRIPS A STEENBERGENSPANJERS GCH LUYTEN JAFM VANDENHEUVEL LPWJ KEYSER A GABREELS FJM WEVERS RA
Citation: A. Verrips et al., 2 NEW MUTATIONS IN THE STEROL 27-HYDROXYLASE GENE IN 2 FAMILIES LEAD TO CEREBROTENDINOUS XANTHOMATOSIS, Human genetics, 98(6), 1996, pp. 735-737

Authors: LEYTEN QH GABREELS FJM RENIER WO TERLAAK HJ
Citation: Qh. Leyten et al., CONGENITAL MUSCULAR-DYSTROPHY - A REVIEW OF THE LITERATURE, Clinical neurology and neurosurgery, 98(4), 1996, pp. 267-280

Authors: MULLENERS WM VANRAVENSWAAY CMA GABREELS FJM HAMEL BCJ VANOORT A SENGERS RCA
Citation: Wm. Mulleners et al., SPINAL MUSCULAR-ATROPHY COMBINED WITH CONGENITAL HEART-DISEASE - A REPORT OF 2 CASES, Neuropediatrics, 27(6), 1996, pp. 333-334

Authors: LEYTEN QH RENIER WO GABREELS FJM BRUNNER HG TERLAAK HJ MULLAART RA
Citation: Qh. Leyten et al., ASSOCIATION OF CONGENITAL MUSCULAR-DYSTROPHY WITH HYPOPLASIA OF THE LATERAL ABDOMINAL-WALL MUSCULATURE AND HYPOPLASIA OF THE EXTERNAL GENITALIA, Neuropediatrics, 27(2), 1996, pp. 108-110

Authors: VANDERWEY LP POLDER TW STEGEMAN DF GABREELSFESTEN AAWM SPAUWEN PHM GABREELS FJM
Citation: Lp. Vanderwey et al., PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY-MONITORED EXPANSION - AN EXPERIMENTAL BASIS FOR FUTURE APPLICATION IN THE MANAGEMENTOF PERIPHERAL-NERVE DEFECTS, Plastic and reconstructive surgery, 97(3), 1996, pp. 568-576

Authors: GABREELSFESTEN AAWM HOOGENDIJK JE MEIJERINK PHS GABREELS FJM BOLHUIS PA VANBEERSUM S KULKENS T NELIS E JENNEKENS FGI DEVISSER M VANENGELEN BGM VANBROECKHOVEN C MARIMAN ECM
Citation: Aawm. Gabreelsfesten et al., 2 DIVERGENT TYPES OF NERVE PATHOLOGY IN PATIENTS WITH DIFFERENT P-0 MUTATIONS IN CHARCOT-MARIE-TOOTH DISEASE, Neurology, 47(3), 1996, pp. 761-765

Authors: WEVERS RA DERIJKVANANDEL JF GABREELS FJM LUDECKE B BLAU N BARTHOLOME K
Citation: Ra. Wevers et al., A NEW CASE OF TYROSINE-HYDROXYLASE DEFICIENCY, Journal of neurochemistry, 66, 1996, pp. 27-27

Authors: VANDOMBURG PHMF GABREELSFESTEN AAWM GABREELS FJM DECOO R RUITENBEEK W WESSELING P TERLAAK H
Citation: Phmf. Vandomburg et al., MITOCHONDRIAL CYTOPATHY PRESENTING AS HEREDITARY SENSORY NEUROPATHY WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, ATAXIA AND FATAL MYOCLONIC EPILEPTIC STATUS, Brain, 119, 1996, pp. 997-1010
Risultati: 1-25 | 26-50 | 51-69