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VANTHOF MA
TOLBOOM JJM
VANSTAVEREN WA
HOFMAN Z
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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
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WESSELING P
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Citation: Ba. Semmekrot et al., INFANTILE MOTOR-NEURON DISEASE WITH AUTONOMIC DYSFUNCTION AND BUNINA BODIES, Acta Neuropathologica, 95(1), 1998, pp. 104-106
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VERKERK PH
VANHOUTEN M
SMIT GPA
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BAKKER HD
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Authors:
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RUITENBEEK W
BENTLAGE HACM
SCHAGGER H
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TERLAAK HJ
MARIMAN ECM
BAKKER MM
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SMEITINK JAM
Citation: Me. Rubiogozalbo et al., FAVORABLE CLINICAL COURSE IN AN INFANT WITH SEVERE DEFICIENCY OF COMPLEX-III OF THE RESPIRATORY-CHAIN COMBINED WITH LESS SEVERE DEFICIENCIES OF COMPLEX-I, COMPLEX-II AND COMPLEX-IV, European journal of pediatrics, 156(12), 1997, pp. 931-934
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SENGERS RCA
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WENDEL U
BENTLAGE HACM
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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
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RUITENBEEK W
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RUITENBEEK W
BENTLAGE HACM
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LEYTEN QH
GABREELS FJM
RENIER WO
VANENGELEN BGM
TERLAAK HJ
SENGERS RCA
THIJSSEN HOM
Citation: Qh. Leyten et al., WHITE-MATTER ABNORMALITIES IN CONGENITAL MUSCULAR-DYSTROPHY, Journal of the neurological sciences, 129(2), 1995, pp. 162-169
Authors:
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JAP PHK
TERLAAK HJ
NONAKA I
BARTH PG
SENGERS RCA
STADHOUDERS AM
RAMAEKERS FCS
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BENTLAGE HACM
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CHOMYN A
ATTARDI G
WALKER JE
SCHAGGER H
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Citation: Hacm. Bentlage et al., MULTIPLE DEFICIENCIES OF MITOCHONDRIAL DNA-ENCODED AND NUCLEAR-ENCODED SUBUNITS OF RESPIRATORY NADH DEHYDROGENASE DETECTED WITH PEPTIDE-SPECIFIC AND SUBUNIT-SPECIFIC ANTIBODIES IN MITOCHONDRIAL MYOPATHIES, Biochimica et biophysica acta. Biomembranes, 1234(1), 1995, pp. 63-73
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RUITENBEEK W
VANLAACK HLJM
JANSSEN AJM
KERKHOF CMC
SENGERS RCA
Citation: W. Sperl et al., MEASUREMENT OF TOTALLY ACTIVATED PYRUVATE-DEHYDROGENASE COMPLEX ACTIVITY IN HUMAN MUSCLE - EVALUATION OF A USEFUL ASSAY, Enzyme & protein, 47(1), 1993, pp. 37-46
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ILES DE
SEGERS B
SENGERS RCA
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HEYTENS L
HALSALL PJ
HOPKINS PM
ELLIS FR
HALLCURRAN JL
STEWART AD
WIERINGA B
Citation: De. Iles et al., GENETIC-MAPPING OF THE BETA(1)-SUBUNIT AND GAMMA-SUBUNIT OF THE HUMANSKELETAL-MUSCLE L-TYPE VOLTAGE-DEPENDENT CALCIUM-CHANNEL ON CHROMOSOME-17Q AND EXCLUSION AS CANDIDATE GENES FOR MALIGNANT HYPERTHERMIA SUSCEPTIBILITY, Human molecular genetics, 2(7), 1993, pp. 863-868
Authors:
ARTS WFM
LOONEN MCB
SENGERS RCA
SLOOFF JL
Citation: Wfm. Arts et al., X-LINKED ATAXIA, WEAKNESS, DEAFNESS, AND LOSS OF VISION IN EARLY-CHILDHOOD WITH A FATAL COURSE, Annals of neurology, 33(5), 1993, pp. 535-539