Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' Wendel, U' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 80 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Scherer, A; Engelbrecht, V; May, P; Neises, G; Wendel, U; Modder, U
      Signal changes of bone marrow in MRI under long-term treatment with granulocyte colony-stimulating factors.

      ROFO-FORTSCHRITTE AUF DEM GEBIET DER RONTGENSTRAHLEN UND DER BILDGEBENDEN VERFAHREN
    2. Scherer, A; Engelbrecht, V; Neises, G; May, P; Balsam, A; Spiekerkotter, U; Wendel, U; Modder, U
      MR imaging of bone marrow in glycogen storage disease type IB in children and young adults

      AMERICAN JOURNAL OF ROENTGENOLOGY
    3. 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
    4. Schadewaldt, P; Bodner-Leidecker, A; Hammen, HW; Wendel, U
      Whole-body L-leucine oxidation in patients with variant form of maple syrup urine disease

      PEDIATRIC RESEARCH
    5. Weglage, J; Pietsch, M; Feldmann, R; Koch, HG; Zschocke, J; Hoffmann, G; Muntau-Heger, A; Denecke, J; Guldberg, P; Guttler, F; Moller, H; Wendel, U; Ullrich, K; Harms, E
      Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia

      PEDIATRIC RESEARCH
    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. Spiekerkotter, U; Schwahn, B; Korall, H; Trefz, FK; Andresen, BS; Wendel, U
      Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spots

      ACTA PAEDIATRICA
    8. Grunewald, S; Imbach, T; Huijben, K; Rubio-Gozalbo, ME; Verrips, A; de Klerk, JBC; Stroink, H; Andel, JFD; Van Hove, JLK; Wendel, U; Matthijs, G; Hennet, T; Jaeken, J; Wevers, RA
      Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis

      ANNALS OF NEUROLOGY
    9. Sperl, W; Murr, C; Skladal, D; Sass, JO; Suormala, T; Baumgartner, R; Wendel, U
      Odd-numbered long-chain fatty acids in propionic acidaemia

      EUROPEAN JOURNAL OF PEDIATRICS
    10. Baethmann, M; Wendel, U; Hoffmann, GF; Gohlich-Ratmann, G; Kleinlein, B; Seiffert, P; Blom, H; Voit, T
      Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolatereductase deficiency

      NEUROPEDIATRICS
    11. Bodner-Leidecker, A; Wendel, U; Saudubray, JM; Schadewaldt, P
      Branched-chain L-amino acid metabolism in classical maple syrup urine disease after orthotopic liver transplantation

      JOURNAL OF INHERITED METABOLIC DISEASE
    12. Schadewaldt, P; Bodner-Leidecker, A; Hammen, HW; Wendel, U
      Formation of L-alloisoleucine in vivo: An L-[C-13]isoleucine study in man

      PEDIATRIC RESEARCH
    13. von Buch, C; Hoppe, B; Luchtrath, M; Wendel, U; Keuth, B; Vierzig, A; Roth, B
      Ornithine transcarbamylase deficiency: hyperammonemic coma after drinking a special "body-building" protein-rich diet

      MONATSSCHRIFT KINDERHEILKUNDE
    14. Schadewaldt, P; Hammen, HW; Loganathan, K; Bodner-Leidecker, A; Wendel, U
      Analysis of concentration and C-13 enrichment of D-galactose in human plasma

      CLINICAL CHEMISTRY
    15. Veiga-Da-Cunha, M; Gerin, I; Chen, YT; Lee, PJ; Leonard, JV; Maire, I; Wendel, U; Vikkula, M; Van Schaftingen, E
      The Putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a

      EUROPEAN JOURNAL OF HUMAN GENETICS
    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. Wendel, U; Saudubray, JM; Bodner, A; Schadewaldt, P
      Liver transplantation in maple syrup urine disease

      EUROPEAN JOURNAL OF PEDIATRICS
    18. Schadewaldt, P; Hammen, HW; Ott, AC; Wendel, U
      Renal clearance of branched-chain L-amino and 2-oxo acids in maple syrup urine disease

      JOURNAL OF INHERITED METABOLIC DISEASE
    19. Herzog, B; Wendel, U; Morris, AAM; Eschrich, K
      Novel mutations in patients with fructose-1,6-bisphosphatase deficiency

      JOURNAL OF INHERITED METABOLIC DISEASE
    20. Huisman, J; Daublin, G; Biggemann, B; Orho, M; Wendel, U
      Glycogen synthase deficiency causing hypoglycemia

      MONATSSCHRIFT KINDERHEILKUNDE
    21. Schadewaldt, P; Bodner-Leidecker, A; Hammen, HW; Wendel, U
      Significance of L-alloisoleucine in plasma for diagnosis of maple syrup urine disease

      CLINICAL CHEMISTRY
    22. KLUIJTMANS LAJ; WENDEL U; STEVENS EMB; VANDENHEUVEL LPWJ; TRIJBELS FJM; BLOM HJ
      IDENTIFICATION OF 4 NOVEL MUTATIONS IN SEVERE METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY

      European journal of human genetics
    23. Schwahn, B; Wendel, U; Schadewaldt, P; Falkenberg, N; Monch, E
      Diurnal changes in plasma amino acids in maple syrup urine disease

      ACTA PAEDIATRICA
    24. NURNBERGER W; LARYEA M; JOCHUM F; WENDEL U; GOBEL U
      HOMOCYSTEINE (HCY) CONCENTRATIONS IN CHILDREN UNDERGOING ALLOGENEIC BLOOD STEM-CELL TRANSPLANTATION (BSCT)

      Bone marrow transplantation
    25. RUBIOGOZALBO ME; RUITENBEEK W; WENDEL U; SENGERS RCA; TRIJBELS JMF; SMEITINK JAM
      SYSTEMIC INFANTILE COMPLEX-I DEFICIENCY WITH FATAL OUTCOME IN 2 BROTHERS

      Neuropediatrics
    26. 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
    27. GRUNEWALD S; HINRICHS F; WENDEL U
      PREGNANCY IN A WOMAN WITH MAPLE-SYRUP-URINE-DISEASE

      Journal of inherited metabolic disease
    28. SCHADEWALDT P; BODNER A; BROSICKE H; HAMMEN HW; WENDEL U
      ASSESSMENT OF WHOLE-BODY L-LEUCINE OXIDATION BY NONINVASIVE L-[1-C-13]LEUCINE BREATH TESTS - A REAPPRAISAL IN PATIENTS WITH MAPLE-SYRUP-URINE-DISEASE, OBLIGATE HETEROZYGOTES, AND HEALTHY-SUBJECTS

      Pediatric research
    29. LARYEA MD; STEINHAGEN F; PAWLICZEK S; WENDEL U
      SIMPLE METHOD FOR THE ROUTINE DETERMINATION OF BETAINE AND N,N-DIMETHYLGLYCINE IN BLOOD AND URINE

      Clinical chemistry
    30. BODNER A; HAMMEN HW; RENN W; WENDEL U; SCHADEWALDT P
      WHOLE-BODY BRANCHED-CHAIN L-AMINO-ACID OXIDATION IN OVERNIGHT FASTED HUMAN-SUBJECTS

      Isotopes in environmental and health studies
    31. SCHADEWALDT P; WENDEL U
      METABOLISM OF BRANCHED-CHAIN AMINO-ACIDS IN MAPLE-SYRUP-URINE-DISEASE

      European journal of pediatrics
    32. 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
    33. ENGELBRECHT V; RASSEK M; HUISMANN J; WENDEL U
      MR AND PROTON MR SPECTROSCOPY OF THE BRAIN IN HYPERHOMOCYSTEINEMIA CAUSED BY METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY

      American journal of neuroradiology
    34. SCHURMANN M; ENGELBRECHT V; LOHMEIER K; LENARD HG; WENDEL U; GARTNER J
      CEREBRAL METABOLIC CHANGES IN BIOTINIDASE DEFICIENCY

      Journal of inherited metabolic disease
    35. GRUNEWALD S; BAKKEREN J; WANDERS RA; WENDEL U
      NEONATAL LETHAL MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY MIMICKING A RESPIRATORY-CHAIN DEFECT

      Journal of inherited metabolic disease
    36. 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
    37. JIRA PE; DEJONG JGN; JANSSENZIJLSTRA FSM; WENDEL U; WEVERS RA
      PITFALLS IN MEASURING PLASMA-CHOLESTEROL IN THE SMITH-LEMLI-OPITZ SYNDROME

      Clinical chemistry
    38. VANBEURDEN EACM; DEGRAAF M; WENDEL U; GITZELMANN R; BERGER R; VANDENBERG IET
      AUTOSOMAL RECESSIVE LIVER PHOSPHORYLASE-KINASE DEFICIENCY CAUSED BY ANOVEL SPLICE-SITE MUTATION IN GENE ENCODING THE LIVER GAMMA-SUBUNIT (PHKG2)

      Biochemical and biophysical research communications
    39. SCHADEWALDT P; WENDEL U; HAMMEN HW
      DETERMINATION OF R-3-METHYL-2-OXOPENTANOATE AND S-3-METHYL-2-OXOPENTANOATE ENANTIOMERS IN HUMAN PLASMA - SUITABLE METHOD FOR LABEL ENRICHMENT ANALYSIS

      Journal of chromatography B. Biomedical applications
    40. BODNER A; RENN W; WENDEL U; SCHADEWALDT P
      COMPARTMENTAL APPROACH FOR EVALUATION OF PLASMA KINETICS AND (CO2)-C-13-EXHALATION AFTER ORAL LOADING WITH L-[1-C-13]LEUCINE

      Isotopes in environmental and health studies
    41. WENDEL U
      CONGENITAL RICKETS - REPLY

      European journal of pediatrics
    42. WENDEL U; LANGENBECK U
      TOWARDS SELF-MONITORING AND SELF-TREATMENT IN PHENYLKETONURIA - A WAYTO BETTER DIET COMPLIANCE

      European journal of pediatrics
    43. HUIZING M; DEPINTO V; RUITENBEEK W; TRIJBELS FJM; VANDENHEUVEL LP; WENDEL U
      IMPORTANCE OF MITOCHONDRIAL TRANSMEMBRANE PROCESSES IN HUMAN MITOCHONDRIOPATHIES

      Journal of bioenergetics and biomembranes
    44. RUITENBEEK W; WENDEL U; HAMEL BCJ; TRIJBELS JMF
      GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS IN DISORDERS OF THE MITOCHONDRIAL ENERGY-METABOLISM

      Journal of inherited metabolic disease
    45. HUIZING M; RUITENBEEK W; THINNES FP; DEPINTO V; WENDEL U; TRIJBELS FJM; SMIT LME; TERLAAK HJ; VANDENHEUVEL LP
      DEFICIENCY OF THE VOLTAGE-DEPENDENT ANION CHANNEL - A NOVEL CAUSE OF MITOCHONDRIOPATHY

      Pediatric research
    46. BENTLAGE HACM; WENDEL U; SCHAGGER H; TERLAAK HJ; JANSSEN AJM; TRIJBELS JMF
      LETHAL INFANTILE MITOCHONDRIAL DISEASE WITH ISOLATED COMPLEX-I DEFICIENCY IN FIBROBLASTS BUT WITH COMBINED COMPLEX-I AND COMPLEX-IV DEFICIENCIES IN MUSCLE

      Neurology
    47. DEUFEL T; MONCH E; PAETZKE I; PRZYREMBEL H; WENDEL U; WILICHOWSKSI E
      DIAGNOSIS AND TREATMENT OF MITOCHONDRIAL (ENCEPHALO)MYOPATHIES - RECOMMENDATIONS BY THE ITSGEMEINSCHAFT-PADIATRISCHE-STOFFWECHSELSTORUNGEN

      Monatsschrift fur Kinderheilkunde
    48. GOLD R; BOGDAHN U; KAPPOS L; TOYKA KV; BAUMGARTNER ER; FOWLER B; WENDEL U
      HEREDITARY DEFECT OF COBALAMIN METABOLISM (HOMOCYSTINURIA AND METHYLMALONIC ACIDURIA) OF JUVENILE-ONSET

      Journal of Neurology, Neurosurgery and Psychiatry
    49. SCHADEWALDT P; WENDEL U; HAMMEN HW
      HUMAN BRANCHED-CHAIN L-AMINO-ACID AMINOTRANSFERASE - ACTIVITY AND SUBCELLULAR-LOCALIZATION IN CULTURED SKIN FIBROBLASTS

      Amino acids
    50. WENDEL U; RUITENBEEK W; BENTLAGE HACM; SENGERS RCA; TRIJBELS JMF
      NEONATAL DETONI-DEBRE-FANCONI-SYNDROME DUE TO A DEFECT IN COMPLEX-IIIOF THE RESPIRATORY-CHAIN

      European journal of pediatrics
    51. HEINDEL W; KUGEL H; WENDEL U; ROTH B; BENZBOHM G
      PROTON MAGNETIC-RESONANCE SPECTROSCOPY REFLECTS METABOLIC DECOMPENSATION IN MAPLE-SYRUP-URINE-DISEASE

      Pediatric radiology
    52. WENDEL U; EISSLER A; SPERL W; SCHADEWALDT P
      ON THE DIFFERENCES BETWEEN URINARY METABOLITE EXCRETION AND ODD-NUMBERED FATTY-ACID PRODUCTION IN PROPIONIC AND METHYLMALONIC ACIDEMIAS

      Journal of inherited metabolic disease
    53. MOURMANS J; BAKKEREN J; DEJONG J; WEVERS R; VANDIGGELEN OP; SUORMALA T; BAUMGARTNER R; WENDEL U
      ISOLATED (BIOTIN-RESISTANT) 3-METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY - 4 SIBS DEVOID OF PATHOLOGY

      Journal of inherited metabolic disease
    54. SCHLENZIG JS; POGGITRAVERT F; LAURENT J; RABIER D; JAN D; WENDEL U; SEWELL AC; REVILLON Y; KAMOUN P; SAUDUBRAY JM
      LIVER-TRANSPLANTATION IN 2 CASES OF PROPIONIC ACIDEMIA

      Journal of inherited metabolic disease
    55. WENDEL U; BAKKEREN J; DEJONG J; BONGAERTS G
      GLUTARIC ACIDURIA MEDIATED BY GUT BACTERIA

      Journal of inherited metabolic disease
    56. ZASS R; LEUPOLD D; FERNANDEZ MA; WENDEL U
      EVALUATION OF PRENATAL TREATMENT IN NEWBORNS WITH COBALAMIN-RESPONSIVE METHYLMALONIC ACIDEMIA

      Journal of inherited metabolic disease
    57. KLOSS S; WENDEL U
      ACUTE INTERMITTENT PORPHYRIA IN CHILDREN - REPLY

      Monatsschrift fur Kinderheilkunde
    58. WEVERS RA; ENGELKE U; WENDEL U; DEJONG JGN; GABREELS FJM; HEERSCHAP A
      STANDARDIZED METHOD FOR HIGH-RESOLUTION H-1-NMR OF CEREBROSPINAL-FLUID

      Clinical chemistry
    59. SCHADEWALDT P; HUMMEL W; WENDEL U; ADELMEYER F
      ENZYMATIC METHOD FOR DETERMINATION OF BRANCHED-CHAIN AMINO-ACID AMINOTRANSFERASE ACTIVITY

      Analytical biochemistry
    60. SCHADEWALDT P; HAMMEN HW; WENDEL U; MATTHIESEN U
      ENZYMATIC-CHEMICAL PREPARATION OF QUINOXALINE DERIVATIVES FROM L-AMINO-ACIDS FOR GAS CHROMATOGRAPHIC-MASS SPECTROMETRIC ANALYSES

      Analytical biochemistry
    61. HINRICHS F; BIGGEMANN B; WENDEL U
      BREAST-FEEDING IN INFANTS WITH PHENYLKETO NURIA

      Klinische Padiatrie
    62. LACAILLE F; POGGITRAVERT F; LAURENT J; JAN D; JOUVET P; RABIER D; REVILLON Y; BRESSON JL; WENDEL U; SAUDUBRAY JM
      LIVER-TRANSPLANTATION FOR PROPIONIC ACIDEMIA IN CHILDREN - PRUDENCE ABOUT A NEW INDICATION

      Hepatology
    63. KRAWINKEL MB; OLDIGS HD; SANTER R; LEHNERT W; WENDEL U; SCHAUB J
      ASSOCIATION OF MALONYL-COA DECARBOXYLASE DEFICIENCY AND HETEROZYGOTE STATE FOR HEMOGLOBIN-C DISEASE

      Journal of inherited metabolic disease
    64. GREGERSEN N; WINTER V; LYONNET S; SAUDUBRAY JM; WENDEL U; JENSEN TG; ANDRESEN BS; KOLVRAA S; BOLUND L; CHRISTENSEN E; BROSS P; LEHNERT W
      MOLECULAR-GENETIC CHARACTERIZATION AND URINARY-EXCRETION PATTERN OF METABOLITES IN 2 FAMILIES WITH MCAD DEFICIENCY DUE TO COMPOUND HETEROZYGOSITY WITH A 13 BASE-PAIR INSERTION IN ONE ALLELE

      Journal of inherited metabolic disease
    65. KLOSS S; VOHRINGER R; WENDEL U
      ACUTE INTERMITTENT PORPHYRIA IN CHILDHOOD

      Monatsschrift fur Kinderheilkunde
    66. WENDEL U
      PHENYLKETONURIA IN ADOLESCENCE - CONTINUE D LOW-PHENYLALANINE DIET WITH SELF-MONITORING

      Monatsschrift fur Kinderheilkunde
    67. HERZIG P; LUDEKING A; HARTLEIB D; ZASS R; VONKRIES R; WENDEL U
      EPIDEMIOLOGY OF THE IDDM IN GERMANY

      Monatsschrift fur Kinderheilkunde
    68. SCHADEWALDT P; BROSICKE H; HAISCH M; MATTHIESEN U; WENDEL U
      LEUCINE OXIDATION IN-VIVO - INTERINDIVIDUAL AND INTRAINDIVIDUAL VARIATION IN HEALTHY-SUBJECTS AS ASSESSED BY ORAL L-[1-C-13]LEUCINE LOADS

      Isotopenpraxis
    69. LARYEA MD; ZASS R; RITGEN J; WENDEL U
      SIMULTANEOUS DETERMINATION OF BETAINE AND N,N-DIMETHYLGLYCINE IN URINE

      Clinica chimica acta
    70. BALLAUFF A; WENDEL U; KUPKE I; KUHNLE U
      A PARTIAL FORM OF PSEUDOHYPOALDOSTERONISM TYPE-I WITHOUT RENAL SODIUMWASTING

      Journal of pediatric endocrinology
    71. MULLER K; KAHN T; WENDEL U
      IS DEMYELINATION A FEATURE OF MAPLE-SYRUP-URINE-DISEASE

      Pediatric neurology
    72. PEINEMANN F; WENDEL U; DANNER DJ
      MOLECULAR-GENETIC CHARACTERIZATION OF MAPLE-SYRUP-URINE-DISEASE IN EUROPEAN FAMILIES

      Biochemical medicine and metabolic biology
    73. BICK U; ULLRICH K; STOBER U; MOLLER H; SCHUIERER G; LUDOLPH AC; OBERWITTLER C; WEGLAGE J; WENDEL U
      WHITE-MATTER ABNORMALITIES IN PATIENTS WITH TREATED HYPERPHENYLALANINEMIA - MAGNETIC-RESONANCE RELAXOMETRY AND PROTON SPECTROSCOPY FINDINGS

      European journal of pediatrics
    74. WENDEL U; ZASS R; LEUPOLD D
      CONTRIBUTION OF ODD-NUMBERED FATTY-ACID OXIDATION TO PROPIONATE PRODUCTION IN NEONATES WITH METHYLMALONIC AND PROPIONIC ACIDEMIAS

      European journal of pediatrics
    75. WENDEL U; SCHROTEN H; BURDACH S; WAHN V
      GLYCOGEN-STORAGE-DISEASE TYPE-IB - INFECTIOUS COMPLICATIONS AND MEASURES FOR PREVENTION

      European journal of pediatrics
    76. PARTSCH CJ; HUMMELINK R; PETER M; SIPPELL WG; OOSTDIJK W; ODINK RJH; DROP SLS; ALBERS N; BRAMSWIG J; DORR H; GONS RJH; HEINRICH U; HENRICHS I; IRLE U; JANSEN M; JOURDAN C; KIESS W; KRAUSE M; KUHNLE U; LEITNER C; LUDERS D; MOLLER H; MUHLENBERG R; VONMUHLENDAHL KE; OTTEN A; OTTEN B; PETERSEN KE; PLUM H; VONPETRYKOWSKI W; ROUWE C; VONSCHNAKENBURG K; STOLECKE H; TIETZE HU; WAELKENS JJJ; WELTERSBACH W; WENDEL U; WIEBEL J; WINKLER L; ZICKLER P; ENGLERT V; HEIDEMANN P
      COMPARISON OF COMPLETE AND INCOMPLETE SUPPRESSION OF PITUITARY-GONADAL ACTIVITY IN GIRLS WITH CENTRAL PRECOCIOUS PUBERTY - INFLUENCE ON GROWTH AND PREDICTED FINAL HEIGHT

      Hormone research
    77. WEISE M; JAMES D; LEITNER CH; HARTMANN KKP; BOHLES HJ; ATTANASIO A; BIERMANNFRANKE H; BEYER P; BOEHLES HJ; BRAEMSWIG J; BRENDEL L; BUTENANDT O; DOERR HG; ENGLERT V; EPPING W; HAHN C; HARTMANN KKP; HAUFFA BP; HECKER W; HEINRICH U; HENRICHS I; HOMOKI J; IRLE U; KNOEBL D; KOLLMANN F; KRUSE K; KUNZE D; LEITNER C; MENKEN U; MUEHLENBERG R; VONMUEHLENDAHL KE; RAGER K; RANKE MB; REINHARDT D; STAHNKE N; STOLECKE H; TIETZE HU; WENDEL U; WILLIG RP
      GLUCOSE-METABOLISM IN ULLRICH-TURNER SYNDROME - LONG-TERM EFFECTS OF THERAPY WITH HUMAN GROWTH-HORMONE

      Hormone research
    78. BIGGEMANN B; ZASS R; WENDEL U
      POSTOPERATIVE METABOLIC DECOMPENSATION IN MAPLE-SYRUP-URINE-DISEASE IS COMPLETELY PREVENTED BY INSULIN

      Journal of inherited metabolic disease
    79. PARTSCH CJ; HUMMELINK R; SIPPELL WG; OOSTDIJK W; ODINK RJH; DROP SLS; BRAMSWIG J; BUTENANDT O; DORR HE; ENGLERT V; GONS RJH; HEIDEMANN P; HEINRICH U; HENRICHS I; IRLE U; JANSEN M; JOURDAN C; KIESS W; KRAUSE M; KUHNLE U; LEITNER C; LUDERS D; MOLLER H; MUHLENBERG R; VONMUHLENDAHL KE; OTTEN A; OTTEN B; PETERSEN KE; PLUM H; VONPETRYKOWSKI W; ROUWE C; VONSCHNAKENBURG K; STOLECKE H; TIETZE HU; WAELKENS JJJ; WELTERSBACH W; WENDEL U; WIEBEL J; WINKLER L; ZICKLER P
      COMPLETE VERSUS INCOMPLETE GONADOTROPIN S UPPRESSION IN GIRLS WITH CENTRAL PRECOCIOUS PUBERTY - IMPACT ON GROWTH AND FINAL HIGHT-PREDICTION

      Monatsschrift fur Kinderheilkunde
    80. WENDEL U; GONZALES J; HUMMEL W
      NEONATAL SCREENING FOR MAPLE-SYRUP-URINE-DISEASE BY AN ENZYME-MEDIATED COLORIMETRIC METHOD

      Clinica chimica acta


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/06/20 alle ore 17:35:54