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    1. White, PC
      Congenital adrenal hyperplasias

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    2. Kuhara, T
      Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas chromatography-mass spectrometry

      JOURNAL OF CHROMATOGRAPHY B
    3. Rashed, MS
      Clinical applications of tandem mass spectrometry: ten years of diagnosis and screening for inherited metabolic diseases

      JOURNAL OF CHROMATOGRAPHY B
    4. Kuhara, T; Ohdoi, C; Ohse, M
      Simple gas chromatographic-mass spectrometric procedure for diagnosing pyrimidine degradation defects for prevention of severe anticancer side effects

      JOURNAL OF CHROMATOGRAPHY B
    5. Boulat, O; McLaren, DG; Arriaga, EA; Chen, DDY
      Separation of free amino acids in human plasma by capillary electrophoresis with laser induced fluorescence: potential for emergency diagnosis of inborn errors of metabolism

      JOURNAL OF CHROMATOGRAPHY B
    6. Jonsen, E; Suhr, OB; Tashima, K; Athlin, E
      Early liver transplantation is essential for familial amyloidotic polyneuropathy patients' quality of life

      AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
    7. Houten, SM; Koster, J; Romeijn, GJ; Frenkel, J; Di Rocco, M; Caruso, U; Landrieu, P; Kelley, RI; Kuis, W; Poll-The, BT; Gibson, KM; Wanders, RJA; Waterham, HR
      Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    8. Cox, KB; Hamm, DA; Millington, DS; Matern, D; Vockley, J; Rinaldo, P; Pinkert, CA; Rhead, WJ; Lindsey, JR; Wood, PA
      Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse

      HUMAN MOLECULAR GENETICS
    9. Trethewey, RN
      Gene discovery via metabolic profiling

      CURRENT OPINION IN BIOTECHNOLOGY
    10. Picca, S; Dionisi-Vici, C; Abeni, D; Pastore, A; Rizzo, C; Orzalesi, M; Sabetta, G; Rizzoni, G; Bartuli, A
      Extracorporeal dialysis in neonatal hyperammonemia: modalities and prognostic indicators

      PEDIATRIC NEPHROLOGY
    11. Holmes, E; Nicholson, JK; Tranter, G
      Metabonomic characterization of genetic variations in toxicological and metabolic responses using probabilistic neural networks

      CHEMICAL RESEARCH IN TOXICOLOGY
    12. Krawczyk, H; Gryff-Keller, A; Gradowska, W; Duran, M; Pronicka, E
      C-13 NMR spectroscopy: a convenient tool for detection of argininosuccinicaciduria

      JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
    13. Baric, I; Fumic, K; Hoffmann, GF
      Inborn errors of metabolism at the turn of the millennium

      CROATIAN MEDICAL JOURNAL
    14. Plochl, E; Plochl, W; Wermuth, B; Roscher, AA
      Variants of inborn errors of metabolism with late onset but nevertheless life threatening course

      KLINISCHE PADIATRIE
    15. Mathias, RS; Kostiner, D; Packman, S
      Hyperammonemia in urea cycle disorders: Role of the nephrologist

      AMERICAN JOURNAL OF KIDNEY DISEASES
    16. Benedetto, B; Madden, R; Kurbanov, A; Braden, G; Freeman, J; Lipkowitz, GS
      Adenine phosphoribosyltransferase deficiency and renal allograft dysfunction

      AMERICAN JOURNAL OF KIDNEY DISEASES
    17. Miano, M; Lanino, E; Gatti, R; Morreale, G; Fondelli, P; Celle, ME; Stroppiano, M; Crescenzi, F; Dini, G
      Four year follow-up of a case of fucosidosis treated with unrelated donor bone marrow transplantation

      BONE MARROW TRANSPLANTATION
    18. Hausler, MG; Jaeken, J; Monch, E; Ramaekers, VT
      Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: Report on two siblings

      NEUROPEDIATRICS
    19. De Kremer, RD; Paschini-Capra, A; Bacman, S; Argarana, C; Civallero, G; Kelley, RI; Guelbert, N; Latini, A; de Halac, IN; Giner-Ayala, A; Johnston, J; Proujansky, R; Gonzalez, I; Depetris-Boldini, C; Oller-Ramirez, A; Angaroni, C; Theaux, RA; Hliba, E; Juaneda, E
      Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Scriver, CR
      Work, the clinician-scientist and human biochemical genetics

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    21. Stadler, S; Gempel, K; Bieger, I; Pontz, BF; Gerbitz, KD; Bauer, MF; Hofmann, S
      Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry

      JOURNAL OF INHERITED METABOLIC DISEASE
    22. Suhr, OB; Lang, K; Wikstrom, L; Anan, I; Ando, Y; El-Salhy, M; Holmgren, G; Tashima, K
      Scavenger treatment of free radical injury in familial amyloidotic polyneuropathy: a study on Swedish transplanted and non-transplanted patients

      SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
    23. Smith, WE; Millington, DS; Koeberl, DD; Lesser, PS
      Glutaric acidemia, type I, missed by newborn screening in an infant with dystonia following promethazine administration

      PEDIATRICS
    24. Takahashi, Y; Sukegawa, K; Aoki, M; Ito, A; Suzuki, K; Sakaguchi, H; Watanabe, M; Isogai, K; Mizuno, S; Hoshi, H; Kuwata, K; Tomatsu, S; Kato, S; Ito, T; Kondo, N; Orii, T
      Evaluation of accumulated mucopolysaccharides in the brain of patients with mucopolysaccharidoses by H-1-magnetic resonance spectroscopy before and after bone marrow transplantation

      PEDIATRIC RESEARCH

    25. Genetic evaluation of stillbirths and neonatal deaths

      OBSTETRICS AND GYNECOLOGY
    26. Plecko, B; Stockler-Ipsiroglu, S
      Macrocephaly as a feature of inborn errors of metabolism

      MONATSSCHRIFT KINDERHEILKUNDE
    27. Prietsch, V; Zschocke, J; Hoffmann, GF
      Diagnosis and therapy for unknown metabolism emergencies. A practical guide

      MONATSSCHRIFT KINDERHEILKUNDE
    28. Summar, M; Tuchman, M
      Proceedings of a consensus conference for the management of patients with urea cycle disorders

      JOURNAL OF PEDIATRICS
    29. Steiner, RD; Cederbaum, SD
      Laboratory evaluation of urea cycle disorders

      JOURNAL OF PEDIATRICS
    30. Summar, M
      Current strategies for the management of neonatal urea cycle disorders

      JOURNAL OF PEDIATRICS
    31. Leonard, JV
      The nutritional management of urea cycle disorders

      JOURNAL OF PEDIATRICS
    32. Batshaw, ML; MacArthur, RB; Tuchman, M
      Alternative pathway therapy for urea cycle disorders: Twenty years later

      JOURNAL OF PEDIATRICS
    33. Berry, GT; Steiner, RD
      Long-term management of patients with urea cycle disorders

      JOURNAL OF PEDIATRICS
    34. Matern, D; Magera, MJ
      Mass spectrometry methods for metabolic and health assessment

      JOURNAL OF NUTRITION
    35. Jones, PM; Moffitt, M; Joseph, D; Harthcock, PA; Boriack, RL; Ibdah, JA; Strauss, AW; Bennett, MJ
      Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain L-3-hydroxyacyl-CoA dehydrogenase: A useful diagnostic aid

      CLINICAL CHEMISTRY
    36. Sweetman, L
      Newborn screening by tandem mass spectrometry: gaining experience

      CLINICAL CHEMISTRY
    37. Zytkovicz, TH; Fitzgerald, EF; Marsden, D; Larson, CA; Shih, VE; Johnson, DM; Strauss, AW; Comeau, AM; Eaton, RB; Grady, GF
      Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: A two-year summary from the New Englandnewborn screening program

      CLINICAL CHEMISTRY
    38. Tang, NLS; Hui, J; Law, LK; To, KF; Mak, TWL; Cheung, KL; Vreken, P; Wanders, RJA; Fok, TF
      Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong

      CLINICA CHIMICA ACTA
    39. Hardy, DT; Preece, MA; Green, A
      Determination of plasma free carnitine by electrospray tandem mass spectrometry

      ANNALS OF CLINICAL BIOCHEMISTRY
    40. de Gennes, JL
      Recent developments in lipid research on atherosclerosis and its prevention - Introduction

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    41. Benlian, P
      Recent advances and new tools in the study of molecular genetics of lipoprotein disorders

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    42. Elgstoen, KBP; Zhao, JY; Anacleto, JF; Jellum, E
      Potential of capillary electrophoresis, tandem mass spectrometry and coupled capillary electrophoresis-tandem mass spectrometry as diagnostic tools

      JOURNAL OF CHROMATOGRAPHY A
    43. Casetta, B; Tagliacozzi, D; Shushan, B; Federici, G
      Development of a method for rapid quantitation of amino acids by liquid chromatography-tandem mass spectrometry (LC-MSMS) in plasma

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    44. Zhang, CH; Xu, KM; Dave, UP; Wang, Y; Matsumoto, I
      Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center

      JOURNAL OF CHROMATOGRAPHY B
    45. Ohie, T; Fu, XW; Iga, M; Kimura, M; Yamaguchi, S
      Gas chromatography-mass spectrometry with tert.-butyldimethylsilyl derivatization: use of the simplified sample preparations and the automated data system to screen for organic acidemias

      JOURNAL OF CHROMATOGRAPHY B
    46. Rinaldo, P; Matern, D
      Disorders of fatty acid transport and mitochondrial oxidation: Challenges and dilemmas of metabolic evaluation

      GENETICS IN MEDICINE
    47. Battaile, KP; Steiner, RD
      Smith-Lemli-Opitz syndrome: The first malformation syndrome associated with defective cholesterol synthesis

      MOLECULAR GENETICS AND METABOLISM
    48. Ibdah, JA; Yang, Z; Bennett, MJ
      Liver disease in pregnancy and fetal fatty acid oxidation defects

      MOLECULAR GENETICS AND METABOLISM
    49. Beatty, ME; Zhang, YH; McCabe, ERB; Steiner, RD
      Fructose-1,6-diphosphatase deficiency and glyceroluria: One possible etiology for GIS

      MOLECULAR GENETICS AND METABOLISM
    50. Liebl, B; Fingerhut, R; Roschinger, W; Muntau, A; Knerr, I; Olgemoller, B; Zapf, A; Roscher, AA
      The bavarian newborn screening model - Concept and first results

      GESUNDHEITSWESEN
    51. Sassa, S
      Hematologic aspects of the porphyrias

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    52. Chen, CY; Chen, YC; Fang, JT; Huang, CC
      Continuous arteriovenous hemodiafiltration in the acute treatment of hyperammonaemia due to ornithine transcarbamylase deficiency

      RENAL FAILURE
    53. Jansen, PLM; Muller, M
      Genetic cholestasis: Lessons from the molecular physiology of bile formation

      CANADIAN JOURNAL OF GASTROENTEROLOGY
    54. Calvo, M; Artuch, R; Macia, E; Luaces, C; Vilaseca, MA; Pou, J; Pineda, M
      Diagnostic approach to inborn errors of metabolism in an emergency unit

      PEDIATRIC EMERGENCY CARE
    55. Costa, CG; Guerand, WS; Struys, EA; Holwerda, U; ten Brink, HJ; de Almeida, IT; Duran, M; Jakobs, C
      Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS

      JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
    56. Mazat, JP; Rossignol, R; Malgat, M; Letellier, T
      Simple models of threshold curves in the expression of inborn errors of metabolism: Application to some experimental observations

      DEVELOPMENTAL NEUROSCIENCE
    57. Fu, XW; Iga, M; Kimura, M; Yamaguchi, S
      Simplified screening for organic acidemia using GC/MS and dried urine filter paper: a study on neonatal mass screening

      EARLY HUMAN DEVELOPMENT
    58. Burlina, AP; Aureli, T; Bracco, F; Conti, F; Battistin, L
      MR spectroscopy: A powerful tool for investigating brain function and neurological diseases

      NEUROCHEMICAL RESEARCH
    59. Malm, D; Halvorsen, DS; Tranebjaerg, L; Sjursen, H
      Immunodeficiency in alpha-mannosidosis: a matched case-control study on immunoglobulins, complement factors, receptor density, phagocytosis and intracellular killing in leucocytes

      EUROPEAN JOURNAL OF PEDIATRICS
    60. Rake, JP; van Spronsen, FJ; Visser, G; Ruitenbeek, W; Schweizer, JJ; Bijleveld, CMA; Peeters, PMJG; de Jong, KP; Slooff, MJH; Reijngoud, DJ; Niezen-Koning, KE; Smit, GPA
      End-stage liver disease as the only consequence of a mitochondrial respiratory chain deficiency: no contra-indication for liver transplantation

      EUROPEAN JOURNAL OF PEDIATRICS
    61. Surtees, R
      Inherited ion channel disorders

      EUROPEAN JOURNAL OF PEDIATRICS
    62. Morris, AAM; Leonard, JV
      Improving the outcome for fatty acid oxidation disorders

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    63. Gustafsson, A; Remberger, M; Winiarski, J; Ringden, O
      Unrelated bone marrow transplantation in children: outcome and a comparison with sibling donor grafting

      BONE MARROW TRANSPLANTATION
    64. Velazquez, A; Vela-Amieva, M; Ciceron-Arellano, I; Ibarra-Gonzalez, I; Perez-Andrade, ME; Olivares-Sandoval, Z; Jimenez-Sanchez, G
      Diagnosis of inborn errors of metabolism

      ARCHIVES OF MEDICAL RESEARCH
    65. de Koning, TJ; Jaeken, J; Pineda, M; Van Maldergem, L; Poll-The, BT; van der Knaap, MS
      Hypomyelination and reversible white matter attenuation in 3-phosphoglycerate dehydrogenase deficiency

      NEUROPEDIATRICS
    66. Praphanproj, V; Boyadjiev, SA; Waber, LJ; Brusilow, SW; Geraghty, MT
      Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemia

      JOURNAL OF INHERITED METABOLIC DISEASE
    67. Burin, M; Dutra, C; Brum, J; Mauricio, T; Amorim, M; Giugliani, R
      Effect of collection, transport, processing and storage of blood specimenson the activity of lysosomal enzymes in plasma and leukocytes

      BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH
    68. Ciani, F; Donati, MA; Tulli, G; Poggi, GM; Pasquini, E; Rosenblatt, DS; Zammarchi, E
      Lethal late onset cblB methylmalonic aciduria

      CRITICAL CARE MEDICINE
    69. Lang, K; Wikstrom, L; Danielsson, A; Tashima, K; Suhr, OB
      Outcome of gastrointestinal complications after liver transplantation for familial amyloidotic polyneuropathy

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    70. Palekar, A
      Effect of pantothenic acid on hippurate formation in sodium benzoate-treated HepG(2) cells

      PEDIATRIC RESEARCH
    71. Lee, B; Yu, H; Jahoor, F; O'Brien, W; Beaudet, AL; Reeds, P
      In vivo urea cycle flux distinguishes and correlates with phenotypic severity in disorders of the urea cycle

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    72. Sander, J; Janzen, N; Sander, S; Melchiors, U; Steuerwald, U
      Neonatal screening for inborn errors of metabolism using tandem mass spectrometry

      MONATSSCHRIFT KINDERHEILKUNDE
    73. Cyr, D; Giguere, R; Giguere, Y; Lemieux, B
      Determination of urinary acylcarnitines: A complementary aid for the high-risk screening of several organic acidurias using a simple and reliable GC/MS-based method

      CLINICAL BIOCHEMISTRY
    74. Mayatepek, E; Zelezny, R; Hoffmann, GF
      Analysis of leukotrienes in cerebrospinal fluid of a reference population and patients with inborn errors of metabolism: further evidence for a pathognomonic profile in LTC4-synthesis deficiency

      CLINICA CHIMICA ACTA
    75. Yoon, HR; Paik, MJ; Shin, HS; Yu, C; Rinaldo, P
      Analysis of plasma free fatty acid cyanomethyl derivatives by GC-NPD for the diagnosis of mitochondrial fatty acid oxidation disorders

      CHROMATOGRAPHIA
    76. Stangl, MJ; Beuers, U; Schauer, R; Lang, T; Gerbes, A; Briegel, J; Da Silva, L; Schildberg, FW; Rau, HG
      Allogenic liver transplantation - a form of "gene therapy" in metabolic diseases. Munich results and review

      CHIRURG
    77. Starck, L; Lovgren, A
      Diagnosis of Smith-Lemli-Opitz syndrome from stored filter paper blood specimens

      ARCHIVES OF DISEASE IN CHILDHOOD
    78. Efrati, C; Masini, A; Merli, M; Valeriano, V; Riggio, O
      Effect of sodium benzoate on blood ammonia response to oral glutamine challenge in cirrhotic patients: A note of caution

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    79. Shigematsu, Y; Hata, I; Kikawa, Y; Mayumi, M; Tanaka, Y; Sudo, M; Kado, N
      Modifications in electrospray tandem mass spectrometry for a neonatal-screening pilot study in Japan

      JOURNAL OF CHROMATOGRAPHY B
    80. Campollo, O; Cortez, R; Odor, A; Munoz, RM; Armendariz-Borunda, J; Alvarez-Tostado, J
      A novel sodium benzoate analog (CH-1) decreases blood ammonia levels in experimental hyperammonemia

      HEPATOLOGY RESEARCH
    81. Trethewey, RN; Krotzky, AJ; Willmitzer, L
      Metabolic profiling: a Rosetta Stone for genomics?

      CURRENT OPINION IN PLANT BIOLOGY
    82. Suhr, OB; Svendsen, IH; Ohlsson, PI; Lendoire, J; Trigo, P; Tashima, K; Ranlov, PJ; Ando, Y
      Impact of age and amyloidosis on thiol conjugation of transthyretin in hereditary transthyretin amyloidosis

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    83. Nyhlin, N; Anan, I; El-Salhy, M; Ando, Y; Suhr, OB
      Endocrine cells in the upper gastrointestinal tract in relation to gastrointestinal dysfunction in patients with familial amyloidotic polyneuropathy

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    84. Tashima, K; Suhr, OB; Ando, Y; Holmgren, G; Yamashita, T; Obayashi, K; Terazaki, H; Uchino, M
      Gastrointestinal dysfunction in familial amyloidotic polyneuropathy (ATTR Val30Met) - comparison of Swedish and Japanese patients

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    85. Yoshino, M; Aoki, K; Akeda, H; Hashimoto, K; Ikeda, T; Inoue, F; Ito, M; Kawamura, M; Kohno, Y; Koga, Y; Kuroda, Y; Maesaka, H; Murakami-Soda, H; Sugiyama, N; Suzuki, Y; Yano, S; Yoshioka, A
      Management of acute metabolic decompensation in maple syrup urine disease:A multi-center study

      PEDIATRICS INTERNATIONAL
    86. Zhou, YQ; Kelly, DP; Strauss, AW; Sims, H; Zhang, ZF
      Characterization of the human very-long-chain acyl-CoA dehydrogenase gene promoter region: A role for activator protein 2

      MOLECULAR GENETICS AND METABOLISM
    87. Chace, DH; Naylor, EW
      Expansion of newborn screening programs using automated tandem mass spectrometry

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    88. Batshaw, ML; Wilson, JM; Raper, S
      Recombinant adenovirus gene transfer in adults with partial ornithine transcarbamylase deficiency (OTCD)

      HUMAN GENE THERAPY
    89. Santamaria, R; Vitagliano, L; Tamasi, S; Izzo, P; Zancan, L; Zagari, A; Salvatore, F
      Novel six-nucleotide deletion in the hepatic fructose-1,6-bisphosphate aldolase gene in a patient with hereditary fructose intolerance and enzyme structure-function implications

      EUROPEAN JOURNAL OF HUMAN GENETICS
    90. Gluckman, E; Rocha, V; Chastang, C
      Cord blood stem cell transplantation

      BAILLIERES CLINICAL HAEMATOLOGY
    91. Chang, MY; Fang, JT; Chen, YC; Huang, CC
      Continuous venovenous haemofiltration in hyperammonaemic coma of an adult with non-diagnosed partial ornithine transcarbamylase deficiency

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    92. Morger, ID; Truttmann, AC; von Vigier, RO; Bettinelli, A; Ramelli, GP; Bianchetti, MG
      Plasma ionized magnesium in tubular disorders with and without total hypomagnesemia

      PEDIATRIC NEPHROLOGY
    93. Brunquell, P; Tezcan, K; DiMario, FJ
      Electroencephalographic findings in ornithine transcarbamylase deficiency

      JOURNAL OF CHILD NEUROLOGY
    94. Naylor, EW; Chace, DH
      Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism

      JOURNAL OF CHILD NEUROLOGY
    95. Wiley, V; Carpenter, K; Wilcken, B
      Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia

      ACTA PAEDIATRICA
    96. Simonsen, H; Jensen, UG
      Technical aspects of neonatal screening using tandem mass spectrometry. Report from the 4th meeting of the International Society for Neonatal Screening

      ACTA PAEDIATRICA
    97. Norgaard-Pedersen, B; Simonsen, H
      Biological specimen banks in neonatal screening

      ACTA PAEDIATRICA
    98. Wanders, RJA
      Peroxisomal disorders: Clinical, biochemical, and molecular aspects

      NEUROCHEMICAL RESEARCH
    99. Saudubray, JM; Touati, G; Delonlay, P; Jouvet, P; Narcy, C; Laurent, J; Rabier, D; Kamoun, P; Jan, D; Revillon, Y
      Liver transplantation in urea cycle disorders

      EUROPEAN JOURNAL OF PEDIATRICS
    100. Saudubray, JM; Touati, G; Delonlay, P; Jouvet, P; Schlenzig, J; Narcy, C; Laurent, J; Rabier, D; Kamoun, P; Jan, D; Revillon, Y
      Liver transplantation in propionic acidaemia

      EUROPEAN JOURNAL OF PEDIATRICS


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Documento generato il 31/10/20 alle ore 03:59:52