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    1. Niers, LEM; Smeitink, JAM; Trijbels, JMF; Sengers, RCA; Janssen, AJM; van den Heuvel, LP
      Prenatal diagnosis of NADH : ubiquinone oxidoreductase deficiency

      PRENATAL DIAGNOSIS
    2. Okhuijsen-Kroes, EJ; Trijbels, JMF; Sengers, RCA; Mariman, E; van den Heuvel, LP; Wendel, U; Koch, G; Smeitink, JAM
      Infantile presentation of the mtDNA A3243G tRNA(Leu(UUR)) mutation

      NEUROPEDIATRICS
    3. Van den Hout, JMP; Reuser, AJJ; de Klerk, JBC; Arts, WF; Smeitink, JAM; Van der Ploeg, AT
      Enzyme therapy for Pompe disease with recombinant human alpha-glucosidase from rabbit milk

      JOURNAL OF INHERITED METABOLIC DISEASE
    4. van der Meer, W; Jakobs, BS; Bocca, G; Smeitink, JAM; Steckhoven, JHS; de Keijzer, MH
      Peripheral blood lymphocyte appearance in a case of I cell disease

      JOURNAL OF CLINICAL PATHOLOGY
    5. Jira, PE; Wanders, RJA; Smeitink, JAM; De Jong, J; Wevers, RA; Oostheim, W; Tuerlings, JHAM; Hennekam, RCM; Sengers, RCA; Waterham, HR
      Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith-Lemli-Opitz syndrome

      ANNALS OF HUMAN GENETICS
    6. Rubio-Gozalbo, ME; Dijkman, KP; van den Heuvel, LP; Sengers, RCA; Wendel, U; Smeitink, JAM
      Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations

      HUMAN MUTATION
    7. Loeffen, JLCM; Smeitink, JAM; Trijbels, JMF; Janssen, AJM; Triepels, RH; Sengers, RCA; van den Heuvel, LP
      Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects

      HUMAN MUTATION
    8. Verrips, A; Willemsen, MAAP; Rubio-Gozalbo, E; De Jong, J; Smeitink, JAM
      Simvastatin and plasma very-long-chain fatty acids in X-linked adrenoleukodystrophy

      ANNALS OF NEUROLOGY
    9. Smeitink, JAM; Sengers, RCA; Trijbels, FJM; van den Heuvel, LP
      Nuclear genes and oxidative phosphorylation disorders: a review

      EUROPEAN JOURNAL OF PEDIATRICS
    10. Rubio-Gozalbo, ME; Sengers, RCA; Trijbels, JMF; Doesburg, WH; Janssen, AJM; Verbeek, ALM; Smeitink, JAM
      A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy

      NEUROPEDIATRICS
    11. Bocca, G; Noordam, C; Wevers, RA; de Jong, JGN; van der Meer, W; de Keijzer, MH; Korver, CRW; Smeitink, JAM
      I-cell disease presenting with severe hypophosphatemia and cardiomyopathy

      NEUROPEDIATRICS
    12. de Rijk-van Andel, JF; Gabreels, FJM; Geurtz, B; Steenbergen-Spanjers, GCH; van den Heuvel, LPWJ; Smeitink, JAM; Wevers, RA
      L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosinehydroxylase deficiency

      NEUROLOGY
    13. Dionisi-Vici, C; Hoffmann, GF; Leuzzi, V; Hoffken, H; Brautigam, C; Rizzo, C; Steebergen-Spanjers, GCH; Smeitink, JAM; Wevers, RA
      Tyrosine hydroxylase deficiency with severe clinical course: Clinical and biochemical investigations and optimization of therapy

      JOURNAL OF PEDIATRICS
    14. Jira, PE; Wevers, RA; de Jong, J; Rubio-Gozalbo, E; Janssen-Zijlstra, FSM; van Heyst, AFJ; Sengers, RCA; Smeitink, JAM
      Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome

      JOURNAL OF LIPID RESEARCH
    15. Budde, SMS; van den Heuvel, LPWJ; Janssen, AJ; Smeets, RJP; Buskens, CAF; DeMeirleir, L; Van Coster, R; Baethmann, M; Voit, T; Trijbels, JMF; Smeitink, JAM
      Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    16. Grunewald, S; Huyben, K; de Jong, JGN; Smeitink, JAM; Rubio, E; Boers, GHJ; Conradt, HS; Wendel, U; Wevers, RA
      beta-trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brain

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    17. Rubio-Gozalbo, ME; Heerschap, A; Trijbels, JMF; De Meirleir, L; Thijssen, HOM; Smeitink, JAM
      Proton MR spectroscopy in a child with pyruvate dehydrogenase complex deficiency

      MAGNETIC RESONANCE IMAGING
    18. Triepels, RH; van den Heuvel, LP; Loeffen, JLCM; Buskens, CAF; Smeets, RJP; Gozalbo, MER; Budde, SMS; Mariman, EC; Wijburg, FA; Barth, PG; Trijbels, JMF; Smeitink, JAM
      Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I

      ANNALS OF NEUROLOGY
    19. van der Knaap, MS; Jakobs, C; Hoffmann, GF; Nyhan, WL; Renier, WO; Smeitink, JAM; Catsman-Berrevoets, CE; Hjalmarson, O; Vallance, H; Sugita, K; Bowe, CM; Herrin, JT; Craigen, WJ; Buist, NRM; Brookfield, DSK; Chalmers, RA
      D-2-hydroxyglutaric aciduria: Biochemical marker or clinical disease entity?

      ANNALS OF NEUROLOGY
    20. Van Kuilenburg, ABP; Vreken, P; Abeling, NGGM; Bakker, HD; Meinsma, R; Van Lenthe, H; De Abreu, RA; Smeitink, JAM; Kayserili, H; Apak, MY; Christensen, E; Holopainen, I; Pulkki, K; Riva, D; Botteon, G; Holme, E; Tulinius, R; Kleijer, WJ; Beemer, FA; Duran, M; Niezen-Koning, KE; Smit, GPA; Jakobs, C; Smit, LME; Moog, U; Spaapen, LJM; Van Gennip, AH
      Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency

      HUMAN GENETICS
    21. Wevers, RA; de Rijk-van Andel, JF; Brautigam, C; Geurtz, B; van den Heuvel, LPWJ; Steenbergen-Spanjers, GCH; Smeitink, JAM; Hoffmann, GF; Gabreels, FJM
      A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)

      JOURNAL OF INHERITED METABOLIC DISEASE
    22. Rubio-Gozalbo, ME; Smeitink, JAM; Ruitenbeek, W; Ter Laak, H; Mullaart, RA; Schuelke, M; Mariman, ECM; Sengers, RCA; Gabreels, FJM
      Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency

      NEUROLOGY
    23. Brautigam, C; Steenbergen-Spanjers, GCH; Hoffmann, GF; Dionisi-Vici, C; van den Heuvel, LPWJ; Smeitink, JAM; Wevers, RA
      Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency

      CLINICAL CHEMISTRY
    24. van Beynum, IM; Smeitink, JAM; den Heijer, M; Pothoff, MTWBT; Blom, HJ
      Hyperhomocysteinemia - A risk factor for ischemic stroke in children

      CIRCULATION
    25. Coenen, MJH; van den Heuvel, LP; Nijtmans, LGJ; Morava, E; Marquardt, I; Girschick, HJ; Trijbels, FJM; Grivell, LA; Smeitink, JAM
      SURFEIT-1 gene analysis and two-dimensional blue native gel electrophoresis in cytochrome c oxidase deficiency

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    26. HERMANS MMP; KROOS MA; SMEITINK JAM; VANDERPLOEG AT; KLEIJER WJ; REUSER AJJ
      GLYCOGEN-STORAGE-DISEASE TYPE-II - GENETIC AND BIOCHEMICAL-ANALYSIS OF NOVEL MUTATIONS IN INFANTILE PATIENTS FROM TURKISH ANCESTRY

      Human mutation
    27. SMEITINK JAM; LOEFFEN JLCM; TRIEPELS RH; SMEETS RJP; TRIJBELS JMF; VANDENHEUVEL LP
      NUCLEAR GENES OF HUMAN COMPLEX I OF THE MITOCHONDRIAL ELECTRON-TRANSPORT CHAIN - STATE-OF-THE-ART

      Human molecular genetics (Print)
    28. VANDENHEUVEL LPWJ; LUITEN B; SMEITINK JAM; RIJKVANANDEL JF; HYLAND K; STEENBERGENSPANJERS GCH; JANSSEN RJT; WEVERS RA
      A COMMON POINT MUTATION IN THE TYROSINE-HYDROXYLASE GENE IN AUTOSOMALRECESSIVE L-DOPA-RESPONSIVE DYSTONIA IN THE DUTCH POPULATION

      Human genetics
    29. RUBIOGOZALBO ME; RUITENBEEK W; WENDEL U; SENGERS RCA; TRIJBELS JMF; SMEITINK JAM
      SYSTEMIC INFANTILE COMPLEX-I DEFICIENCY WITH FATAL OUTCOME IN 2 BROTHERS

      Neuropediatrics
    30. HUIZING M; RUITENBEEK W; VANDENHEUVEL LP; DOLCE V; IACOBAZZI V; SMEITINK JAM; PALMIERI F; TRIJBELS JMF
      HUMAN MITOCHONDRIAL TRANSMEMBRANE METABOLITE CARRIERS - TISSUE DISTRIBUTION AND ITS IMPLICATION FOR MITOCHONDRIAL DISORDERS

      Journal of bioenergetics and biomembranes
    31. HUIZING M; WENDEL U; RUITENBEEK W; IACOBAZZI V; IJLST L; VEENHUIZEN P; SAVELKOUL P; VANDENHEUVEL LP; SMEITINK JAM; WANDERS RJA; TRIJBELS JMF; PALMIERI F
      CARNITINE-ACYLCARNITINE CARRIER DEFICIENCY - IDENTIFICATION OF THE MOLECULAR DEFECT IN A PATIENT

      Journal of inherited metabolic disease
    32. BRAUTIGAM C; WEVERS RA; JANSEN RJT; SMEITINK JAM; DERIJKVANANDEL JF; GABREELS FJM; HOFFMANN GF
      BIOCHEMICAL HALLMARKS OF TYROSINE-HYDROXYLASE DEFICIENCY

      Clinical chemistry
    33. Loeffen, JLCM; Triepels, RH; van den Heuvel, LP; Schuelke, M; Buskens, CAF; Smeets, RJP; Trijbels, JMF; Smeitink, JAM
      cDNA of eight nuclear encoded subunits of NADH : ubiquinone oxidoreductase: Human complex I cDNA characterization completed

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    34. CASALE CH; CASALS N; PIE J; ZAPATER N; PEREZCERDA C; MERINERO B; MARTINEZPARDO M; GARCIAPENAS JJ; GARCIAGONZALEZ JM; LAMA R; POLLTHE BT; SMEITINK JAM; WANDERS RJA; UGARTE M; HEGARDT FG
      A NONSENSE MUTATION IN THE EXON-2 OF THE 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A LYASE (HL) GENE PRODUCING 3 MATURE MESSENGER-RNAS IS THE MAIN CAUSE OF 3-HYDROXY-3-METHYLGLUTARIC ACIDURIA IN EUROPEAN MEDITERRANEAN PATIENTS

      Archives of biochemistry and biophysics
    35. WATERHAM HR; WIJBURG FA; HENNEKAM RCM; VREKEN P; POLLTHE BT; DORLAND L; DURAN M; JIRA PE; SMEITINK JAM; WEVERS RA; WANDERS RJA
      SMITH-LEMLI-OPITZ-SYNDROME IS CAUSED BY MUTATIONS IN THE 7-DEHYDROCHOLESTEROL REDUCTASE GENE

      American journal of human genetics
    36. VANDERPUT NMJ; GABREELS F; STEVENS EMB; SMEITINK JAM; TRIJBELS FJM; ESKES TKAB; VANDENHEUVEL LP; BLOM HJ
      A 2ND COMMON MUTATION IN THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE- AN ADDITIONAL RISK FACTOR FOR NEURAL-TUBE DEFECTS

      American journal of human genetics
    37. VANDERPUT NMJ; THOMAS CMG; ESKES TKAB; TRIJBELS FJM; STEEGERSTHEUNISSEN RPM; MARIMAN ECM; DEGRAAFHESS A; SMEITINK JAM; BLOM HJ
      ALTERED FOLATE AND VITAMIN-B-12 METABOLISM IN FAMILIES WITH SPINA-BIFIDA OFFSPRING

      Quarterly Journal of Medicine
    38. DEKEIJZER MH; JAKOBS BS; BRANDTS RW; HOFS MTW; TRIJBELS FJM; SMEITINK JAM
      RAPID AND RELIABLE MEASUREMENT OF HIGHLY ELEVATED BLOOD AMMONIA CONCENTRATIONS IN CHILDREN

      European journal of clinical chemistry and clinical biochemistry
    39. HUIZING M; RUITENBEEK W; DEPINTO V; THINNES F; TRIJBELS JMF; VANDENHEUVEL LP; SMEITINK JAM
      THE VOLTAGE-DEPENDENT ANION CHANNEL (VDAC) IN HUMAN MITOCHONDRIAL DISORDERS

      The FASEB journal
    40. RUITENBEEK W; HUIZING M; PALMIERI F; TRIJBELS JMF; VANDENHEUVEL LP; SMEITINK JAM
      INVOLVEMENT OF MITOCHONDRIAL-MEMBRANE CARRIERS IN HUMAN (ENCEPHALO-)MYOPATHIES

      The FASEB journal
    41. RUBIOGOZALBO ME; RUITENBEEK W; BENTLAGE HACM; SCHAGGER H; SENGERS RCA; TRIJBELS JMF; TERLAAK HJ; MARIMAN ECM; BAKKER MM; DEJAGER J; SMEITINK JAM
      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
    42. TRIJBELS FJM; RUITENBEEK W; HUIZING M; WENDEL U; SMEITINK JAM; SENGERS RCA
      DEFECTS IN THE MITOCHONDRIAL ENERGY-METABOLISM OUTSIDE THE RESPIRATORY-CHAIN AND THE PYRUVATE-DEHYDROGENASE COMPLEX

      Molecular and cellular biochemistry
    43. AUSEMS MGEM; BAKKER E; BERGER R; DURAN M; VANDIGGELEN OP; KEULEMANS JLM; DEVALK HW; KNEPPERS ALJ; DORLAND L; ESKES PF; BEEMER FA; POLLTHE BT; SMEITINK JAM
      ASYMPTOMATIC AND LATE-ONSET ORNITHINE TRANSCARBAMYLASE DEFICIENCY CAUSED BY A A208T MUTATION - CLINICAL, BIOCHEMICAL AND DNA ANALYSES IN A 4-GENERATION FAMILY

      American journal of medical genetics
    44. MULDERS TMT; BERGMAN DJW; POLLTHE BT; SMIT GPA; BREIMER DD; MULDER GJ; DURAN M; SMEITINK JAM
      ABNORMAL GLUTATHIONE CONJUGATION IN PATIENTS WITH TYROSINEMIA TYPE-I

      Journal of inherited metabolic disease
    45. MOURMANS J; WENDEL U; BENTLAGE HACM; TRIJBELS JMF; SMEITINK JAM; DECOO IFM; GABREELS FJM; SENGERS RCA; RUITENBEEK W
      CLINICAL HETEROGENEITY IN RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY INCHILDHOOD

      Journal of the neurological sciences
    46. SCHRIJVERWIELING I; VANRENS GHMB; WITTEBOLPOST D; SMEITINK JAM; DEJAGER JP; DEKLERK HBC; VANLITH GHM
      RETINAL DYSTROPHY IN LONG-CHAIN 3-HYDROXY-ACYL-COA DEHYDROGENASE-DEFICIENCY

      British journal of ophthalmology
    47. BLAU N; DEKLERK JBC; THONY B; HEIZMANN CW; KIERAT L; SMEITINK JAM; DURAN M
      TETRAHYDROBIOPTERIN LOADING TEST IN XANTHINE DEHYDROGENASE AND MOLYBDENUM COFACTOR DEFICIENCIES

      Biochemical and molecular medicine
    48. MOTLEY AM; TABAK HF; SMEITINK JAM; POLLTHE BT; BARTH PG; WANDERS RJA
      NON-RHIZOMELIC AND RHIZOMELIC CHONDRODYSPLASIA PUNCTATA WITHIN A SINGLE COMPLEMENTATION GROUP

      Biochimica et biophysica acta. Molecular basis of disease
    49. DEVALK HW; VANEEDEN MKG; BANGA JD; VANDERGRIEND R; DEGROOT E; HAAS FJLM; MEUWISSEN OJAT; DURAN M; SMEITINK JAM; POLLTHE BT; DEKLERK JBC
      EVALUATION OF THE PRESENCE OF PREMATURE ATHEROSCLEROSIS IN ADULTS WITH HETEROZYGOSITY FOR CYSTATHIONINE-BETA-SYNTHASE DEFICIENCY

      Stroke
    50. BERGMAN AJIW; VANDERKNAAP MS; SMEITINK JAM; DURAN M; DORLAND L; VALK J; POLLTHE BT
      MAGNETIC-RESONANCE-IMAGING AND SPECTROSCOPY OF THE BRAIN IN PROPIONICACIDEMIA - CLINICAL AND BIOCHEMICAL CONSIDERATIONS

      Pediatric research
    51. BUESA C; PIE J; BARCELO A; CASALS N; MASCARO C; CASALE CH; HARO D; DURAN M; SMEITINK JAM; HEGARDT FG
      ABERRANTLY SPLICED MESSENGER-RNAS OF THE 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A LYASE (HL) GENE WITH A DONOR SPLICE-SITE POINT MUTATION PRODUCE HEREDITARY HL DEFICIENCY

      Journal of lipid research
    52. VANDIGGELEN OP; ZAREMBA J; HE W; KEULEMANS JLM; BOER AM; REUSER AJJ; AUSEMS MGEM; SMEITINK JAM; KOWALCZYK J; PRONICKA E; ROKICKI D; TARNOWSKADZIDUSZKO E; KNEPPERS ALJ; BAKKER E
      ASYMPTOMATIC AND LATE-ONSET ORNITHINE TRANSCARBAMYLASE (OTC) DEFICIENCY IN MALES OF A 5-GENERATION FAMILY, CAUSED BY AN A208T MUTATION

      Clinical genetics
    53. AUSEMS MGEM; KROOS MA; VANDERKRAAN M; SMEITINK JAM; KLEIJER WJ; VANAMSTEL HKP; REUSER AJJ
      HOMOZYGOUS DELETION OF EXON-18 LEADS TO DEGRADATION OF THE LYSOSOMAL ALPHA-GLUCOSIDASE PRECURSOR AND TO THE INFANTILE FORM OF GLYCOGEN-STORAGE-DISEASE TYPE-II

      Clinical genetics
    54. VANDERSIJSBOS CJM; DIEPSTRATEN CM; JUYN JA; PLAISIER M; GILTAY JC; VANSPRONSEN FJ; SMIT GPA; BERGER R; SMEITINK JAM; POLLTHE BT; VANAMSTEL JKP
      PHENYLKETONURIA IN THE NETHERLANDS - 93-PERCENT OF THE MUTATIONS ARE DETECTED BY SINGLE-STRAND CONFORMATION ANALYSIS

      Human heredity
    55. ESPEEL M; MANDEL H; POGGI F; SMEITINK JAM; WANDERS RJA; KERCKAERT I; SCHUTGENS RBH; SAUDUBRAY JM; POLLTHE BT; ROELS F
      PEROXISOME MOSAICISM IN THE LIVERS OF PEROXISOMAL DEFICIENCY PATIENTS

      Hepatology
    56. ESPEEL M; ROELS F; GIROS M; MANDEL H; PELTIER A; POGGI F; POLLTHE BT; SMEITINK JAM; VANMALDERGEM L; SANTOS MJ
      IMMUNOLOCALIZATION OF A 43 KDA PEROXISOMAL MEMBRANE-PROTEIN IN THE LIVER OF PATIENTS WITH GENERALIZED PEROXISOMAL DISORDERS

      European journal of cell biology
    57. DEHINGH YCM; MEYER J; FISCHER JC; BERGER R; SMEITINK JAM; DENKAMP JAFO
      DIRECT MEASUREMENT OF LIPID-PEROXIDATION IN SUBMITOCHONDRIAL PARTICLES

      Biochemistry
    58. VANDENBERG IET; VANBEURDEN EACM; MALINGRE HEM; VANAMSTEL HKP; POLLTHE BT; SMEITINK JAM; LAMERS WH; BERGER R
      X-LINKED LIVER PHOSPHORYLASE-KINASE DEFICIENCY IS ASSOCIATED WITH MUTATIONS IN THE HUMAN LIVER PHOSPHORYLASE-KINASE ALPHA-SUBUNIT

      American journal of human genetics
    59. BEEKMAN RP; HOFSTEE N; SMEITINK JAM; POLLTHE BT; DURAN M
      RETT-SYNDROME IN A PATIENT WITH MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY

      European journal of pediatrics
    60. FOURNIER B; SMEITINK JAM; DORLAND L; BERGER R; SAUDUBRAY JM; POLLTHE BT
      PEROXISOMAL DISORDERS - A REVIEW

      Journal of inherited metabolic disease
    61. BERGMAN AJIW; DONCKERWOLCKE RAMG; DURAN M; SMEITINK JAM; MOUSSON B; VIANEYSABAN C; POLLTHE BT
      RATE-DEPENDENT DISTAL RENAL TUBULAR-ACIDOSIS AND CARNITINE PALMITOYLTRANSFERASE-I DEFICIENCY

      Pediatric research
    62. ESPEEL M; HEIKOOP JC; SMEITINK JAM; BEEMER FA; DECRAEMER D; VANDENBERG M; HASHIMOTO T; WANDERS RJA; SCHUTGENS RBH; POLLTHE BT; ROELS F
      CYTOPLASMIC CATALASE AND GHOSTLIKE PEROXISOMES IN THE LIVER FROM A CHILD WITH ATYPICAL CHONDRODYSPLASIA PUNCTATA

      Ultrastructural pathology
    63. DURAN M; BAUMGARTNER ER; SUORMALA TM; BRUINVIS L; DORLAND L; SMEITINK JAM; POLLTHE BT
      CEREBROSPINAL-FLUID ORGANIC-ACIDS IN BIOTINIDASE DEFICIENCY

      Journal of inherited metabolic disease
    64. SMEITINK JAM; FISCHER JC; RUITENBEEK W; DURAN M; HOFKAMP M; BENTLAGE HAJM; POLLTHE BT
      SUDDEN INFANT DEATH ASSOCIATED WITH DEFECTIVE OXIDATIVE-PHOSPHORYLATION

      Lancet
    65. DORLAND L; POLLTHE BT; DURAN M; SMEITINK JAM; BERGER R
      PHENYLPYRUVATE, FETAL DAMAGE, AND MATERNAL PHENYLKETONURIA SYNDROME

      Lancet


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/05/20 alle ore 12:18:30