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Results: 1-24 |
Results: 24
GENETIC-CHARACTERISTICS OF MYOADENYLATE DEAMINASE DEFICIENCY
Authors: VERZIJL HTFM VANENGELEN BGM LUYTEN JAFM STEENBERGEN GCH VANDENHEUVEL LPWJ TERLAAK HJ PADBERG GW WEVERS RA
Citation: Htfm. Verzijl et al., GENETIC-CHARACTERISTICS OF MYOADENYLATE DEAMINASE DEFICIENCY, Annals of neurology, 44(1), 1998, pp. 140-143
LAMININ-ALPHA(2) (MEROSIN), BETA-DYSTROGLYCAN, ALPHA-SARCOGLYCAN (ADHALIN), AND DYSTROPHIN EXPRESSION IN CONGENITAL MUSCULAR-DYSTROPHIES - AN IMMUNOHISTOCHEMICAL STUDY
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
COMPLEX REGIONAL PAIN SYNDROME TYPE-I (RSD) - PATHOLOGY OF SKELETAL-MUSCLE AND PERIPHERAL-NERVE
Authors: VANDERLAAN L TERLAAK HJ GABREELSFESTEN A GABREELS F GORIS RJA
Citation: L. Vanderlaan et al., COMPLEX REGIONAL PAIN SYNDROME TYPE-I (RSD) - PATHOLOGY OF SKELETAL-MUSCLE AND PERIPHERAL-NERVE, Neurology, 51(1), 1998, pp. 20-25
MULTICORE MYOPATHY WITH RESTRICTIVE CARDIOMYOPATHY
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
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
Authors: RUBIOGOZALBO ME RUITENBEEK W BENTLAGE HACM SCHAGGER H SENGERS RCA TRIJBELS JMF TERLAAK HJ MARIMAN ECM BAKKER MM DEJAGER J 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
SOFT-TISSUE REPAIR CAPACITY AFTER OXYGEN-DERIVED FREE RADICAL-INDUCEDDAMAGE IN ONE HINDLIMB OF THE RAT
Authors: VANDERLAAN L OYEN WJG VERHOFSTAD AAJ TAN ECTH TERLAAK HJ GABREELSFESTEN A HENDRIKS T GORIS RJA
Citation: L. Vanderlaan et al., SOFT-TISSUE REPAIR CAPACITY AFTER OXYGEN-DERIVED FREE RADICAL-INDUCEDDAMAGE IN ONE HINDLIMB OF THE RAT, The Journal of surgical research, 72(1), 1997, pp. 60-69
PARKINSONISM-MELAS OVERLAP SYNDROME-ASSOCIATED WITH A MITOCHONDRIAL CYTOCHROME-B FRAMESHIFT MUTATION
Authors: DECOO RFM RENIER WO RUITENBEEK W TERLAAK HJ BAKKER M VANOOST BA SMEETS HJM
Citation: Rfm. Decoo et al., PARKINSONISM-MELAS OVERLAP SYNDROME-ASSOCIATED WITH A MITOCHONDRIAL CYTOCHROME-B FRAMESHIFT MUTATION, American journal of human genetics, 61(4), 1997, pp. 1790-1790
CONGENITAL MUSCULAR-DYSTROPHY - A REVIEW OF THE LITERATURE
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
ASSOCIATION OF CONGENITAL MUSCULAR-DYSTROPHY WITH HYPOPLASIA OF THE LATERAL ABDOMINAL-WALL MUSCULATURE AND HYPOPLASIA OF THE EXTERNAL GENITALIA
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
DEFICIENCY OF THE VOLTAGE-DEPENDENT ANION CHANNEL - A NOVEL CAUSE OF MITOCHONDRIOPATHY
Authors: HUIZING M RUITENBEEK W THINNES FP DEPINTO V WENDEL U TRIJBELS FJM SMIT LME TERLAAK HJ VANDENHEUVEL LP
Citation: M. Huizing et al., DEFICIENCY OF THE VOLTAGE-DEPENDENT ANION CHANNEL - A NOVEL CAUSE OF MITOCHONDRIOPATHY, Pediatric research, 39(5), 1996, pp. 760-765
LETHAL INFANTILE MITOCHONDRIAL DISEASE WITH ISOLATED COMPLEX-I DEFICIENCY IN FIBROBLASTS BUT WITH COMBINED COMPLEX-I AND COMPLEX-IV DEFICIENCIES IN MUSCLE
Authors: BENTLAGE HACM WENDEL U SCHAGGER H TERLAAK HJ JANSSEN AJM TRIJBELS JMF
Citation: Hacm. Bentlage et al., LETHAL INFANTILE MITOCHONDRIAL DISEASE WITH ISOLATED COMPLEX-I DEFICIENCY IN FIBROBLASTS BUT WITH COMBINED COMPLEX-I AND COMPLEX-IV DEFICIENCIES IN MUSCLE, Neurology, 47(1), 1996, pp. 243-248
MYOPATHOLOGY IN PATIENTS WITH A NOONAN PHENOTYPE
Authors: DEBOODE WP SEMMEKROT BA TERLAAK HJ VANDERBURGT CJAM DRAAISMA JMT LOMMEN EJP SENGERS RCA VANWIJKHOEK JM
Citation: Wp. Deboode et al., MYOPATHOLOGY IN PATIENTS WITH A NOONAN PHENOTYPE, Acta Neuropathologica, 92(6), 1996, pp. 597-602
RIMMED BASOPHILIC VACUOLES AND FILAMENTOUS INCLUSIONS IN NEUROMUSCULAR DISORDERS
Authors: JONGEN PJH TERLAAK HJ STADHOUDERS AM
Citation: Pjh. Jongen et al., RIMMED BASOPHILIC VACUOLES AND FILAMENTOUS INCLUSIONS IN NEUROMUSCULAR DISORDERS, Neuromuscular disorders, 5(1), 1995, pp. 31-38
INCLUSION-BODY MYOSITIS RESPONDING TO LONG-TERM CHLORAMBUCIL TREATMENT
Authors: JONGEN PJH TERLAAK HJ VANDEPUTTE LBA
Citation: Pjh. Jongen et al., INCLUSION-BODY MYOSITIS RESPONDING TO LONG-TERM CHLORAMBUCIL TREATMENT, Journal of rheumatology, 22(3), 1995, pp. 576-578
WHITE-MATTER ABNORMALITIES IN CONGENITAL MUSCULAR-DYSTROPHY
Authors: 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
IMMUNOPHENOTYPING OF CONGENITAL MYOPATHIES - DISORGANIZATION OF SARCOMERIC, CYTOSKELETAL AND EXTRACELLULAR-MATRIX PROTEINS
Authors: VANDERVEN PFM JAP PHK TERLAAK HJ NONAKA I BARTH PG SENGERS RCA STADHOUDERS AM RAMAEKERS FCS
Citation: Pfm. Vanderven et al., IMMUNOPHENOTYPING OF CONGENITAL MYOPATHIES - DISORGANIZATION OF SARCOMERIC, CYTOSKELETAL AND EXTRACELLULAR-MATRIX PROTEINS, Journal of the neurological sciences, 129(2), 1995, pp. 199-213
CONGENITAL MUSCULAR-DYSTROPHY AND SEVERE CENTRAL-NERVOUS-SYSTEM ATROPHY IN 2 SIBLINGS
Authors: LEYTEN QH BARTH PG GABREELS FJM RENKAWEK K RENIER WO GABREELSFESTEN AAWM TERLAAK HJ SMITS MG
Citation: Qh. Leyten et al., CONGENITAL MUSCULAR-DYSTROPHY AND SEVERE CENTRAL-NERVOUS-SYSTEM ATROPHY IN 2 SIBLINGS, Acta Neuropathologica, 90(6), 1995, pp. 650-656
COXSACKIE B1 VIRUS-INDUCED MURINE MYOSITIS - RELATIONSHIP OF DISEASE SEVERITY TO VIRUS DOSE AND ANTIVIRAL ANTIBODY-RESPONSE
Authors: JONGEN PJH HEESSEN FWA TERLAAK HJ GALAMA JMD GABREELS FJM
Citation: Pjh. Jongen et al., COXSACKIE B1 VIRUS-INDUCED MURINE MYOSITIS - RELATIONSHIP OF DISEASE SEVERITY TO VIRUS DOSE AND ANTIVIRAL ANTIBODY-RESPONSE, Neuromuscular disorders, 4(1), 1994, pp. 17-23
COXSACKIE B1 VIRUS-INDUCED MURINE MYOSITIS - A CORRELATIVE STUDY OF MUSCULAR LESIONS AND SEROLOGICAL CHANGES
Authors: JONGEN PJH HEESSEN FWA BERGMANN I DEWAAL RMW TERLAAK HJ GALAMA JMD VANVENROOIJ WJ GABREELS FJM VANDEPUTTE LB BERDEN JHM
Citation: Pjh. Jongen et al., COXSACKIE B1 VIRUS-INDUCED MURINE MYOSITIS - A CORRELATIVE STUDY OF MUSCULAR LESIONS AND SEROLOGICAL CHANGES, Journal of autoimmunity, 7(6), 1994, pp. 727-737
THE OLFACTORY-BULB IN ALZHEIMER-DISEASE - A MORPHOLOGIC STUDY OF NEURON LOSS, TANGLES, AND SENILE PLAQUES IN RELATION TO OLFACTION
Authors: TERLAAK HJ RENKAWEK K VANWORKUM FPA
Citation: Hj. Terlaak et al., THE OLFACTORY-BULB IN ALZHEIMER-DISEASE - A MORPHOLOGIC STUDY OF NEURON LOSS, TANGLES, AND SENILE PLAQUES IN RELATION TO OLFACTION, Alzheimer disease and associated disorders, 8(1), 1994, pp. 38-48
MYOTONIC-DYSTROPHY KINASE IS LOCALIZED AT NEUROMUSCULAR AND MYOTENDINOUS JUNCTIONS
Authors: VANDERVEN PFM JANSEN G PERRYMAN MB VANKUPPEVELT THMSM TERLAAK HJ JAP PHK EPSTEIN HF WIERINGA B
Citation: Pfm. Vanderven et al., MYOTONIC-DYSTROPHY KINASE IS LOCALIZED AT NEUROMUSCULAR AND MYOTENDINOUS JUNCTIONS, Journal of muscle research and cell motility, 15(2), 1994, pp. 180-180
MYOTONIC-DYSTROPHY KINASE IS A COMPONENT OF NEUROMUSCULAR-JUNCTIONS
Authors: VANDERVEN PFM JANSEN G VANKUPPEVELT THMSM PERRYMAN MB LUPA M DUNNE PW TERLAAK HJ JAP PHK VEERKAMP JH EPSTEIN HF WIERINGA B
Citation: Pfm. Vanderven et al., MYOTONIC-DYSTROPHY KINASE IS A COMPONENT OF NEUROMUSCULAR-JUNCTIONS, Human molecular genetics, 2(11), 1993, pp. 1889-1894
DEFICIENCY OF NA+ K+-ATPASE AND SARCOPLASMIC-RETICULUM CA2+-ATPASE INSKELETAL-MUSCLE AND CULTURED MUSCLE-CELLS OF MYOTONIC-DYSTROPHY PATIENTS/
Authors: BENDERS AAGM TIMMERMANS JAH OOSTERHOF A TERLAAK HJ VANKUPPEVELT THMSM WEVERS RA VEERKAMP JH
Citation: Aagm. Benders et al., DEFICIENCY OF NA+ K+-ATPASE AND SARCOPLASMIC-RETICULUM CA2+-ATPASE INSKELETAL-MUSCLE AND CULTURED MUSCLE-CELLS OF MYOTONIC-DYSTROPHY PATIENTS/, Biochemical journal, 293, 1993, pp. 269-274
CONGENITAL MUSCULAR-DYSTROPHY - A STUDY ON THE VARIABILITY OF MORPHOLOGICAL-CHANGES AND DYSTROPHIN DISTRIBUTION IN MUSCLE BIOPSIES
Authors: LEYTEN QH TERLAAK HJ GABREELS FJM RENIER WO RENKAWEK K SENGERS RCA
Citation: Qh. Leyten et al., CONGENITAL MUSCULAR-DYSTROPHY - A STUDY ON THE VARIABILITY OF MORPHOLOGICAL-CHANGES AND DYSTROPHIN DISTRIBUTION IN MUSCLE BIOPSIES, Acta Neuropathologica, 86(4), 1993, pp. 386-392
Risultati: 1-24 |