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    1. Prip-Buus, C; Thuillier, L; Abadi, N; Prasad, C; Dilling, L; Klasing, J; Demaugre, F; Greenberg, CR; Haworth, JC; Droin, V; Kadhom, N; Gobin, S; Kamoun, P; Girard, J; Bonnefont, JP
      Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite community

      MOLECULAR GENETICS AND METABOLISM
    2. Kamoun, P
      Mental retardation in Down syndrome: a hydrogen sulfide hpothesis

      MEDICAL HYPOTHESES
    3. De Lonlay, P; Benelli, C; Fouque, F; Ganguly, A; Aral, B; Dionisi-Vici, C; Touati, G; Heinrichs, C; Rabier, D; Kamoun, P; Robert, JJ; Stanley, C; Saudubray, JM
      Hyperinsulinism and hyperammonemia syndrome: Report of twelve unrelated patients

      PEDIATRIC RESEARCH
    4. Belardinelli, MC; Chabli, A; Chadefaux-Vekemans, B; Kamoun, P
      Urinary sulfur compounds in Down syndrome

      CLINICAL CHEMISTRY
    5. Baumgartner, MR; Hu, CAA; Almashanu, S; Steel, G; Obie, C; Aral, B; Rabier, D; Kamoun, P; Saudubray, JM; Valle, D
      Hyperammonemia with reduced ornithine, citrulline, arginine and proline: anew inborn error caused by a mutation in the gene encoding Delta(1)-pyrroline-5-carboxylate synthase

      HUMAN MOLECULAR GENETICS
    6. Thuillier, L; Sevin, C; Demaugre, F; Brivet, M; Rabier, D; Droin, V; Aupetit, J; Abadi, N; Kamoun, P; Saudubray, JM; Bonnefont, JP
      Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient

      NEUROMUSCULAR DISORDERS
    7. Kamoun, P
      Future Earth observation missions and environmental risks

      SURVEYS IN GEOPHYSICS
    8. Saudubray, JM; De Lonlay, P; Touati, G; Martin, D; Nassogne, MC; Castelnau, P; Sevin, C; Laborde, C; Baussan, C; Brivet, M; Vassault, A; Rabier, D; Bonnefont, JP; Kamoun, P
      Genetic hypoglycaemia in infancy and childhood: Pathophysiology and diagnosis

      JOURNAL OF INHERITED METABOLIC DISEASE
    9. Kraus, JP; Janosik, M; Kozich, V; Mandell, R; Shih, V; Sperandeo, MP; Sebastio, G; de Franchis, R; Andria, G; Kluijtmans, LAJ; Blom, H; Boers, GHJ; Gordon, RB; Kamoun, P; Tsai, MY; Kruger, WD; Koch, HG; Ohura, T; Gaustadnes, M
      Cystathionine beta-synthase mutations in homocystinuria

      HUMAN MUTATION
    10. 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
    11. 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
    12. Saudubray, JM; Martin, D; de Lonlay, P; Touati, G; Poggi-Travert, F; Bonnet, D; Jouvet, P; Boutron, M; Slama, A; Vianey-Saban, C; Bonnefont, JP; Rabier, D; Kamoun, P; Brivet, M
      Recognition and management of fatty acid oxidation defects: A series of 107 patients

      JOURNAL OF INHERITED METABOLIC DISEASE
    13. Kamoun, P; Campbell, D; Pettengill, G; Shapiro, I
      Radar observations of three comets and detection of echoes from one: P/Grigg-Skjellerup

      PLANETARY AND SPACE SCIENCE
    14. Quere, I; Paul, V; Rouillac, C; Janbon, C; London, J; Demaille, J; Kamoun, P; Dufier, JL; Abitbol, M; Chasse, JF
      Spatial and temporal expression of the cystathionine beta-synthase gene during early human development

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    15. LIU G; ARAL B; ZABOT MT; KAMOUN P; CEBALLOSPICOT I
      THE MOLECULAR-BASIS OF HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASEDEFICIENCY IN FRENCH FAMILIES - REPORT OF 2 NOVEL MUTATIONS

      Human mutation
    16. KAMOUN P; RABIER D; SAUDUBRAY JM
      MUSCULAR ORIGIN OF HYPERAMMONEMIA

      European journal of pediatrics
    17. MERINERO B; PEREZCERDA C; GARCIA MJ; CHADEFAUXVEKEMANS B; KAMOUN P; TONETTI C; ZITTOUN J; JAKOBS C; UGARTE M
      RELIABILITY OF BIOCHEMICAL PARAMETERS USED IN PRENATAL-DIAGNOSIS OF COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA

      Prenatal diagnosis
    18. RABIER D; DIRY C; ROTIG A; RUSTIN P; HERON B; BARDET J; PARVY P; PONSOT G; MARSAC C; SAUDUBRAY JM; MUNNICH A; KAMOUN P
      PERSISTENT HYPOCITRULLINAEMIA AS A MARKER FOR MTDNA NARP T-8993 G-MUTATION

      Journal of inherited metabolic disease
    19. Thuillier, L; Chadefaux-Vekemans, B; Bonnefont, JP; Kara, A; Aupetit, J; Rochette, C; Montalescot, G; Couty, MC; Kamoun, P; Ankri, A
      Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

      JOURNAL OF INHERITED METABOLIC DISEASE
    20. Coude, M; Aupetit, J; Zabot, MT; Kamoun, P; Chadefaux-Vekemans, B
      Four novel mutations at the cystathionine beta-synthase locus causing homocystinuria

      JOURNAL OF INHERITED METABOLIC DISEASE
    21. KAMOUN P; ARAL B; SAUDUBRAY JM
      A NEW INHERITED METABOLIC DISEASE - DELTA -1-PYRROLINE 5-CARBOXYLATE SYNTHETASE DEFICIENCY

      Bulletin de l'Academie nationale de medecine
    22. ARAL B; COUDE M; LONDON J; AUPETIT J; CHASSE JF; ZABOT MT; CHADEFAUXVEKEMANS B; KAMOUN P
      2 NOVEL MUTATIONS (K384E AND L539S) IN THE C-TERMINAL MOIETY OF THE CYSTATHIONINE BETA-SYNTHASE PROTEIN IN 2 FRENCH PYRIDOXINE-RESPONSIVE HOMOCYSTINURIA PATIENTS

      Human mutation
    23. ARAL B; KAMOUN P
      THE PROLINE BIOSYNTHESIS IN LIVING ORGANISMS

      Amino acids
    24. CHASSE JF; PAUL V; ESCANEZ R; KAMOUN P; LONDON J
      HUMAN CYSTATHIONINE BETA-SYNTHASE - GENE ORGANIZATION AND EXPRESSION OF DIFFERENT 5'-ALTERNATIVE SPLICING

      Mammalian genome
    25. MIRCHER C; SALABELLE A; PEETERS MA; RABIER D; PARVY P; KAMOUN P; LEJEUNE J
      PLASMA AND URINARY AMINO-ACID-CONCENTRATI ONS IN DOWNS-SYNDROME - EFFECT OF AGE

      Archives de pediatrie
    26. MONTALESCOT G; ANKRI A; VEKEMANS B; BLACHER J; PHILIPPE F; DROBINSKI G; KAMOUN P; THOMAS D
      HOMOCYSTEINE IS INCREASED IN PATIENTS WITH DIFFUSE ATHEROSCLEROSIS

      Journal of the American College of Cardiology
    27. JUNGERS P; CHAUVEAU P; BANDIN O; CHADEFAUX B; AUPETIT J; LABRUNIE M; DESCAMPSLATSCHA B; KAMOUN P
      HYPERHOMOCYSTEINEMIA IS ASSOCIATED WITH ATHEROSCLEROTIC OCCLUSIVE ARTERIAL ACCIDENTS IN PREDIALYSIS CHRONIC-RENAL-FAILURE PATIENTS

      Mineral and electrolyte metabolism
    28. ANKRI A; BONNEFONT JP; CHADEFAUXVEKEMANS B; MOSTEFA AK; AUPETIT J; COUTY MC; MONTALESCOT G; KAMOUN P; THUILLIER L
      THE 677C-T MUTATION IN THE METHYLENE-TETRAHYDROFOLATE REDUCTASE GENE IS NOT RELATED TO HYPERHOMOCYSTEINEMIA IN THROMBOTIC DISEASE

      Thrombosis and haemostasis
    29. CHASSE JF; PAUL V; ESCANEZ R; PARIS D; CASANOVA M; PALY E; KAMOUN P; LONDON J
      HUMAN CYSTATHIONINE-B SYNTHASE GENE - GENOMIC ORGANIZATION AND EXPRESSION

      Cytogenetics and cell genetics
    30. MONTALESCOT G; ANKRI A; CHADEFAUXVEKEMANS B; BLACHER J; PHILIPPE F; DROBINSKI G; BENZIDIA R; KAMOUN P; THOMAS D
      PLASMA HOMOCYSTEINE AND THE EXTENT OF ATHEROSCLEROSIS IN PATIENTS WITH CORONARY-ARTERY DISEASE

      International journal of cardiology
    31. ABITBOL M; QUERE I; JAMBON P; CHASSE JF; KOBETZ A; MARCHANT D; KAMOUN P; DUFIER P; DUFIER JL
      VEGF AND KDR GENE-EXPRESSION IN THE HUMAN DEVELOPING EYE

      Investigative ophthalmology & visual science
    32. ANKRI A; MONTALESCOT G; CHADEFAUX B; BLACHER J; COUTY MC; KAMOUN P; THOMAS D; BINET JL
      MILD HYPERHOMOCYSTEINEMIA IS A GRADUATE RISK FACTOR FOR ARTERIAL AND VENOUS THROMBOSIS DISEASE

      Blood
    33. ARAL B; BENELLI C; AITGHEZALA G; AMESSOU M; FOUQUE F; MAUNOURY C; CREAU N; KAMOUN P; MARSAC C
      MUTATIONS IN PDX1, THE HUMAN LIPOYL-CONTAINING COMPONENT-X OF THE PYRUVATE-DEHYDROGENASE COMPLEX GENE ON CHROMOSOME 11P1, IN CONGENITAL LACTIC-ACIDOSIS

      American journal of human genetics
    34. FAUREDELANEF L; QUERE I; CHASSE JF; GUERASSIMENKO O; LESAULNIER M; BELLET H; ZITTOUN J; KAMOUN P; COHEN D
      METHYLENETETRAHYDROFOLATE REDUCTASE THERMOLABILE VARIANT AND HUMAN LONGEVITY

      American journal of human genetics
    35. ARAL B; DESAINTBASILE G; ALGARAWI S; KAMOUN P; CEBALLOSPICOT I
      NOVEL NONSENSE MUTATION IN THE HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE GENE AND NONRANDOM X-INACTIVATION CAUSING LESCH-NYHAN SYNDROME IN A FEMALE-PATIENT

      Human mutation
    36. JUNGERS P; CHAUVEAU P; CHADEFAUX B; AUPETIT J; LABRUNIE M; DESCAMPSLATSCHA B; KAMOUN P
      HYPERHOMOCYSTEINEMIA IS ASSOCIATED WITH ARTERIAL OCCLUSIVE ACCIDENTS IN PREDIALYSIS CHRONIC-RENAL-FAILURE (CFR) PATIENTS

      Journal of the American Society of Nephrology
    37. CHAUVEAU P; CHADEFAUX B; KOLKO A; BONETE R; BANDIN O; AUPETIT J; KAMOUN P; POIGNET JL
      HYPERHOMOCYSTEINEMIA IN HEMODIALYZED PATIENTS - EFFECT OF FOLATE SUPPLEMENTATION AND DIALYSIS MEMBRANES

      Journal of the American Society of Nephrology
    38. LIU G; MAUNOURY C; KAMOUN P; ARAL B
      ASSIGNMENT OF THE HUMAN GENE ENCODING THE DELTA(1)-PYRROLINE-5-CARBOXYLATE SYNTHETASE (P5CS) TO 10Q24.3 BY IN-SITU HYBRIDIZATION

      Genomics
    39. ARAL B; SCHLENZIG JB; LIU G; KAMOUN P
      DATABASE CLONING HUMAN DELTA(1)-PYRROLINE-5-CARBOXYLATE SYNTHETASE (P5CS) CDNA - A BIFUNCTIONAL ENZYME CATALZING THE FIRST 2 STEPS IN PROLINE SYNTHESIS

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    40. CHAUVEAU P; CHADEFAUX B; COUDE M; AUPETIT J; KAMOUN P; JUNGERS P
      LONG-TERM FOLIC-ACID (BUT NOT PYRIDOXINE) SUPPLEMENTATION LOWERS ELEVATED PLASMA HOMOCYSTEINE LEVEL IN CHRONIC-RENAL-FAILURE

      Mineral and electrolyte metabolism
    41. VANDERMEER SB; POGGI F; SPADA M; BONNEFONT JP; OGIER H; HUBERT P; DEPONDT E; RAPOPORT D; RABIER D; CHARPENTIER C; PARVY P; BARDET J; KAMOUN P; SAUDUBRAY JM
      CLINICAL OUTCOME AND LONG-TERM MANAGEMENT OF 17 PATIENTS WITH PROPIONIC ACIDEMIA

      European journal of pediatrics
    42. RABIER D; CHADEFAUXVEKEMANS B; OURY JF; AUPETIT J; BARDET J; GASQUET M; MERHAND E; PARVY P; KAMOUN P
      GESTATIONAL AGE-RELATED REFERENCE VALUES FOR AMNIOTIC-FLUID AMINO-ACIDS - A USEFUL TOOL FOR PRENATAL-DIAGNOSIS OF AMINOACIDOPATHIES

      Prenatal diagnosis
    43. POGGITRAVERT F; MARTIN D; DEVILLEMEUR TB; BONNEFONT JP; VASSAULT A; RABIER D; CHARPENTIER C; KAMOUN P; MUNNICH A; SAUDUBRAY JM
      METABOLIC INTERMEDIATES IN LACTIC-ACIDOSIS - COMPOUNDS, SAMPLES AND INTERPRETATION

      Journal of inherited metabolic disease
    44. ANKRI A; CHADEFAUXVEKEMANS B; MOSTEFA AK; AUPETIT J; THUILLIER L; COUTY MC; MONTALESCOT G; KAMOUN P; BONNEFORT JP
      DOES THE PREVALENT MUTATION 677-]T IN THE METHYLENE-TETRAHYDROFOLATE REDUCTASE GENE CONTRIBUTE TO HYPERHOMOCYSTEINEMIA RELATED TO VASCULAR-DISEASE

      Blood
    45. BLACHER J; MONTALESCOT G; ANKRI A; CHADEFAUXVEKEMANS B; BENZIDIA R; GROSGOGEAT Y; KAMOUN P; THOMAS D
      HYPERHOMOCYSTEINAEMIA IN CORONARY-ARTERY DISEASE - RESULTS OF A STUDYOF 102 PATIENTS

      Archives des maladies du coeur et des vaisseaux
    46. RABIER D; KAMOUN P
      METABOLISM OF CITRULLINE IN MAN

      Amino acids
    47. DELABESSE E; ARAL S; KAMOUN P; VARET B; TURHAN AG
      QUANTITATIVE NONRADIOACTIVE CLONALITY ANALYSIS OF HUMAN LEUKEMIC-CELLS AND PROGENITORS USING THE HUMAN ANDROGEN RECEPTOR (AR) GENE

      Leukemia
    48. QUEREL; MOLHOSABATIER P; DUPUY E; CHADEFAUX B; KAMOUN P; JANBON C; TOBELEM G
      HYPERHOMOCYSTEINEMIA AND DEEP VENOUS THROMBOSIS

      Thrombosis and haemostasis
    49. SCHLENZIG JS; CHARPENTIER C; RABIER D; KAMOUN P; SEWELL AC; HARPEY JP
      L-CARNITINE - A WAY TO DECREASE CELLULAR TOXICITY OF IFOSFAMIDE

      European journal of pediatrics
    50. KAMOUN P; FENSOM AH; SHIN YS; BAKKER E; COLOMBO JP; MUNNICH A; BIRD S; CANINI S; HUIJMANS JGM; CHADEFAUXVEKEMANS B; WHITFIELD AE; KLEIJER WJ
      PRENATAL-DIAGNOSIS OF THE UREA CYCLE DISEASES - A SURVEY OF THE EUROPEAN CASES

      American journal of medical genetics
    51. 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
    52. RABIER D; BARDET J; PARVY P; POGGI F; BRIVET M; SAUDUBRAY JM; KAMOUN P
      DO CRITERIA EXIST FROM URINARY ORGANIC-ACIDS TO DISTINGUISH BETA-OXIDATION DEFECTS

      Journal of inherited metabolic disease
    53. CANDITO M; RICHELME C; PARVY P; DAGEVILLE C; APPERT A; BEKRI S; RABIER D; CHAMBON P; MARIANI R; KAMOUN P
      ABNORMAL ALPHA-AMINOADIPIC ACID EXCRETION IN A NEWBORN WITH A DEFECT IN PLATELET-AGGREGATION AND ANTENATAL CEREBRAL-HEMORRHAGE

      Journal of inherited metabolic disease
    54. PARVY P; BARDET J; GASQUET M; RABIER D; KAMOUN P
      STABILITY OF FREE AMINO-ACIDS IN SULFOSALICYLIC FILTRATES

      Clinical chemistry
    55. PARVY P; BARDET J; CHADEFAUXVEKEMANS B; RABIER D; GASQUET M; AUPETIT J; KAMOUN P
      FREE AMINO-ACIDS IN AMNIOTIC-FLUID AND THE PRENATAL-DIAGNOSIS OF HOMOCYSTINURIA WITH METHYLMALONIC ACIDURIA

      Clinical chemistry
    56. PARVY P; BARDET J; RABIER D; KAMOUN P
      A SCHEME FOR THE INTERPRETATION OF PRIMARY AND SECONDARY DISTURBANCESOF PLASMA AND URINARY AMINO-ACID PROFILES - A POSSIBLE WAY TO AN EXPERT-SYSTEM

      Clinica chimica acta
    57. CHASSE JF; PALY E; PARIS D; PAUL V; SINET PM; KAMOUN P; LONDON J
      GENOMIC ORGANIZATION OF THE HUMAN CYSTATHIONINE BETA-SYNTHASE GENE - EVIDENCE FOR VARIOUS CDNAS

      Biochemical and biophysical research communications
    58. JUNGERS P; CHAUVEAU P; CHADEFAUX B; COUDE M; AUPETIT J; KAMOUN P
      HYPERHOMOCYSTEINEMIA IN CHRONIC-RENAL-FAILURE PATIENTS - BENEFICIAL EFFECT OF FOLATE SUPPLEMENTATION

      Journal of the American Society of Nephrology
    59. MASSY ZA; CHADEFAUXVEKEMANS B; CHEVALIER A; BADER CA; DRUEKE TB; LEGENDRE C; LACOUR B; KAMOUN P; KREIS H
      HYPERHOMOCYSTEINAEMIA - A SIGNIFICANT RISK FACTOR FOR CARDIOVASCULAR-DISEASE IN RENAL-TRANSPLANT RECIPIENTS

      Nephrology, dialysis, transplantation
    60. POGGITRAVERT F; HERON B; DEVILLEMEUR TB; SPADA M; JOUVET P; CHARPENTIER C; RABIER D; KAMOUN P; SAUDUBRAY JM
      DIAGNOSIS OF COMA OF METABOLIC ORIGIN IN CHILDREN

      Archives de pediatrie
    61. POGGI F; RABIER D; VASSAULT A; CHARPENTIER C; KAMOUN P; SAUDUBRAY JM
      LABORATORY INVESTIGATIONS PROTOCOL FOR TH E DIAGNOSIS OF HEREDITARY METABOLIC DISORDERS

      Archives de pediatrie
    62. MONTAGUTELLI X; LALOUETTE A; COUDE M; KAMOUN P; FOREST M; GUENET JL
      AKU, A MUTATION OF THE MOUSE HOMOLOGOUS TO HUMAN ALKAPTONURIA, MAPS TO CHROMOSOME-16

      Genomics
    63. CHADEFAUXVEKEMANS B; ROLLAND MO; LYONNET S; RABIER D; DIVRY P; KAMOUN P
      PRENATAL-DIAGNOSIS OF COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA (COBALAMIN CBLC OR CBLD MUTANT)

      Prenatal diagnosis
    64. KAMOUN P; PARVY P; RABIER D; BARDET J; DEVILLEMEUR TB; SAUDUBRAY JM
      DICARBOXYLIC AMINOACIDURIA

      Journal of inherited metabolic disease
    65. VANDERMEER SB; POGGI F; SPADA M; BONNEFONT JP; OGIER H; HUBERT P; DEPONDT E; RAPOPORT D; RABIER D; CHARPENTIER C; PARVY P; BARDET J; KAMOUN P; SAUDUBRAY JM
      CLINICAL OUTCOME OF LONG-TERM MANAGEMENT OF PATIENTS WITH VITAMIN-B-12-UNRESPONSIVE METHYLMALONIC ACIDEMIA

      The Journal of pediatrics
    66. DELABESSE E; ARAL B; VARET B; KAMOUN P; TURHAN AG
      QUANTITATIVE NONRADIOACTIVE CLONALITY ANALYSIS IN LEUKEMIC-CELLS AND PROGENITORS USING FLUORESCENT PRIMERS FOR THE HUMAN ANDROGEN RECEPTOR (HUMARA) GENE

      Blood
    67. MULLER F; PARVY P; DOMMERGUES M; LORTATJACOB S; DUMEZ Y; KAMOUN P
      FREE AMINO-ACIDS IN FETAL URINE AND PROGN OSIS OF FETAL BILATERAL OBSTRUCTIVE UROPATHIES

      Annales de biologie clinique
    68. COUDE M; MONTAGUTELLI X; GUENET JL; KAMOUN P
      HOMOGENTISIC ACID OXIDASE ACTIVITY IN HOMOZYGOUS AND HETEROZYGOUS ALKAPTONURIC MICE

      Annales de biologie clinique
    69. MONASTIRI K; RABIER D; KAMOUN P
      PRENATAL-DIAGNOSIS OF ORNITHINE - TRANSCARBAMYLASE DEFICIENCY - RESULTS IN SPF(ASH) MICE

      Prenatal diagnosis
    70. CANDITO M; BEBIN B; VIANEYSABAN C; RABIER D; BEKRI S; SEBAG F; CHAMBON P; KAMOUN P
      ARGINASE DEFICIENCY IN 2 BROTHERS

      Journal of inherited metabolic disease
    71. KAABACHI N; LARNAOUT A; RABIER D; JAKOBS C; BELAL S; HENTATI F; PARVEY P; BARDET J; BENHAMIDA M; MEBAZAA A; KAMOUN P
      FAMILIAL ENCEPHALOPATHY AND L-2-HYDROXYGLUTARIC ACIDURIA

      Journal of inherited metabolic disease
    72. CHAUVEAU P; CHADEFAUX B; COUDE M; AUPETIT J; HANNEDOUCHE T; KAMOUN P; JUNGERS P
      HYPERHOMOCYSTEINEMIA, A RISK FACTOR FOR ATHEROSCLEROSIS IN CHRONIC UREMIC PATIENTS

      Kidney international
    73. BIENVENU T; ANKRI A; CHADEFAUX B; MONTALESCOT G; KAMOUN P
      ELEVATED TOTAL PLASMA HOMOCYSTEINE, A RISK FACTOR FOR THROMBOSIS - RELATION TO COAGULATION AND FIBRINOLYTIC PARAMETERS

      Thrombosis research
    74. PARVY P; BARDET J; RABIER D; GASQUET M; KAMOUN P
      INTRALABORATORY AND INTERLABORATORY QUALITY-CONTROL FOR ASSAY OF AMINO-ACIDS IN BIOLOGICAL-FLUIDS - 14 YEARS OF THE FRENCH EXPERIENCE

      Clinical chemistry
    75. KAMOUN P
      PRENATAL-DIAGNOSIS OF THE UREA CYCLE DISEASES - A SURVEY OF THE EUROPEAN CASES

      Annales de biologie clinique
    76. ROZET JM; PELET A; RABIER D; SEGUES B; SAUGIER P; LYONNET S; BONAITI C; SAUDUBRAY JM; KAMOUN P; MUNNICH A
      PRENATAL-DIAGNOSIS AND GENETIC-COUNSELING IN ORNITHINE TRANSCARBAMYLASE DEFICIENCY

      Annales de biologie clinique


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Documento generato il 12/08/20 alle ore 00:45:18