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    1. De Freitas, JM; Meneghini, R
      Iron and its sensitive balance in the cell

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    2. Zeviani, M; Klopstock, T
      Mitochondrial disorders

      CURRENT OPINION IN NEUROLOGY
    3. Roy, CN; Andrews, NC
      Recent advances in disorders of iron metabolism: mutations, mechanisms andmodifiers

      HUMAN MOLECULAR GENETICS
    4. Lill, R; Kispal, G
      Mitochondrial ABC transporters

      RESEARCH IN MICROBIOLOGY
    5. Fleming, MD; Campagna, DR; Haslett, JN; Trenor, CC; Andrews, NC
      A mutation in a mitochondrial transmembrane protein is responsible for thepleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice

      GENES & DEVELOPMENT
    6. Kumar, A; Jazieh, AR
      Case report of sideroblastic anemia caused by ingestion of coins

      AMERICAN JOURNAL OF HEMATOLOGY
    7. Sladky, JT
      Histopathological features of peripheral nerve and muscle in mitochondrialdisease

      SEMINARS IN NEUROLOGY
    8. Meunier, B
      Site-directed mutations in the mitochondrially encoded subunits I and III of yeast cytochrome oxidase

      BIOCHEMICAL JOURNAL
    9. Wimazal, F; Sperr, WR; Kundi, M; Meidlinger, P; Fonatsch, C; Jordan, JH; Thalhammer-Scherrer, R; Schwarzinger, I; Geissler, K; Lechner, K; Valent, P
      Prognostic value of lactate dehydrogenase activity in myelodysplastic syndromes

      LEUKEMIA RESEARCH
    10. Aleem, A; Murray, JA
      Spherocytosis preceding the development of myelodysplasia

      CLINICAL AND LABORATORY HAEMATOLOGY
    11. Walker, BL; Tiong, JWC; Jefferies, WA
      Iron metabolism in mammalian cells

      INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 211
    12. Friedman, JS; Rebel, VI; Derby, R; Bell, K; Huang, TT; Kuypers, FA; Epstein, CJ; Burakoff, SJ
      Absence of mitochondrial superoxide dismutase results in a murine hemolytic anemia responsive to therapy with a catalytic antioxidant

      JOURNAL OF EXPERIMENTAL MEDICINE
    13. Cheltsov, AV; Barber, MJ; Ferreira, GC
      Circular permutation of 5-aminolevulinate synthase - Mapping the polypeptide chain to its function

      JOURNAL OF BIOLOGICAL CHEMISTRY
    14. Kim, R; Saxena, S; Gordon, DM; Pain, D; Dancis, A
      J-domain protein, Jac1p, of yeast mitochondria required for iron homeostasis and activity of Fe-S cluster proteins

      JOURNAL OF BIOLOGICAL CHEMISTRY
    15. Andrews, NC
      Iron metabolism: Iron deficiency and iron overload

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    16. Andrews, NC
      Iron homeostasis: Insights from genetics and animal models

      NATURE REVIEWS GENETICS
    17. Kook, H; Kim, CJ; Yoon, WS; Ryang, DW; Hwang, TJ
      Successful allogeneic bone marrow transplantation for childhood-onset refractory anemia with ringed sideroblasts

      JOURNAL OF KOREAN MEDICAL SCIENCE
    18. Yamamoto, M; Nakajima, O
      Animal models for X-linked sideroblastic anemia

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    19. Shirihai, OS; Gregory, T; Yu, CN; Orkin, SH; Weiss, MJ
      ABC-me: a novel mitochondrial transporter induced by GATA-1 during erythroid differentiation

      EMBO JOURNAL
    20. Gardais, J
      Dyshaemopoiesis in adults: a practical classification for diagnosis and management

      LEUKEMIA RESEARCH
    21. Gattermann, N
      From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes

      LEUKEMIA RESEARCH
    22. Germing, U; Gattermann, N; Strupp, C; Aivado, M; Aul, C
      Validation of the WHO proposals for a new classification of primary myelodysplastic syndromes: a retrospective analysis of 1600 patients

      LEUKEMIA RESEARCH
    23. Sheth, S; Brittenham, GM
      Genetic disorders affecting proteins of iron metabolism: Clinical implications

      ANNUAL REVIEW OF MEDICINE
    24. Prodan, CI; Holland, NR
      CNS demyelination from zinc toxicity?

      NEUROLOGY
    25. Porea, TJ; Belmont, JW; Mahoney, DH
      Zinc-induced anemia and neutropenia in an adolescent

      JOURNAL OF PEDIATRICS
    26. Mitsuhashi, N; Miki, T; Senbongi, H; Yokoi, N; Yano, H; Miyazaki, M; Nakajima, N; Iwanaga, T; Yokoyama, Y; Shibata, T; Seino, S
      MTABC3, a novel mitochondrial ATP-binding cassette protein involved in iron homeostasis

      JOURNAL OF BIOLOGICAL CHEMISTRY
    27. Edgar, AJ; Polak, JM
      Molecular cloning of the human and murine 2-amino-3-ketobutyrate coenzyme A ligase cDNAs

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    28. Dzikaite, V; Kanopka, A; Brock, JH; Kazlauskas, A; Melefors, O
      A novel endoproteolytic processing activity in mitochondria of erythroid cells and the role in heme synthesis

      BLOOD
    29. Hassan, HA; Netchvolodoff, C; Raufman, JP
      Zinc-induced copper deficiency in a coin swallower

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    30. Hofhaus, G; Gattermann, N
      Mitochondria harbouring mutant mtDNA - a cuckoo in the nest?

      BIOLOGICAL CHEMISTRY
    31. Lill, R; Diekert, K; Kaut, A; Lange, H; Pelzer, W; Prohl, C; Kispal, G
      The essential role of mitochondria in the biogenesis of cellular iron-sulfur proteins

      BIOLOGICAL CHEMISTRY
    32. Sadlon, TJ; Dell'Oso, T; Surinya, KH; May, BK
      Regulation of erythroid 5-aminolevulinate synthase expression during erythropoiesis

      INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
    33. Barceloux, DG
      Zinc

      JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY
    34. Harigae, H; Furuyama, K; Kudo, K; Hayashi, N; Yamamoto, M; Sassa, S; Sasaki, T
      A novel mutation of the erythroid-specific delta-aminolevulinate synthase gene in a patient with non-inherited pyridoxine-responsive sideroblastic anemia

      AMERICAN JOURNAL OF HEMATOLOGY
    35. Wimazal, F; Sperr, WR; Horny, HP; Carroll, V; Binder, BR; Fonatsch, C; Walchshofer, S; Fodinger, M; Schwarzinger, I; Samorapoompichit, P; Chott, A; Dvorak, AM; Lechner, K; Valent, P
      Hyperfibrinolysis in a case of myelodysplastic syndrome with leukemic spread of mast cells

      AMERICAN JOURNAL OF HEMATOLOGY
    36. Nakajima, O; Takahashi, S; Harigae, H; Furuyama, K; Hayashi, N; Sassa, S; Yamamoto, M
      Heme deficiency in erythroid lineage causes differentiation arrest and cytoplasmic iron overload

      EMBO JOURNAL
    37. Kispal, G; Csere, P; Prohl, C; Lill, R
      The mitochondrial proteins Atm1p and Nfs1p are essential for biogenesis ofcytosolic Fe/S proteins

      EMBO JOURNAL
    38. Krahenbuhl, S; Kleinle, S; Henz, S; Leibundgut, K; Liechti, S; Zimmermann, A; Wiesmann, U
      Microvesicular steatosis, hemosiderosis and rapid development of liver cirrhosis in a patient with Pearson's syndrome

      JOURNAL OF HEPATOLOGY
    39. Bader-Meunier, B; Mielot, F; Breton-Gorius, J; Cramer, E; Guichard, J; Landrieu, P; Dommergues, JP; Tchernia, G
      Hematologic involvement in mitochondrial cytopathies in childhood: A retrospective study of bone marrow smears

      PEDIATRIC RESEARCH
    40. Bessho, F; Ohnishi, H; Tabuchi, K; Kobayashi, M; Hayashi, Y
      Significance of electron-dense deposits in the mitochondrial matrix of erythroid precursors in aplastic anaemia and myelodysplastic syndrome

      BRITISH JOURNAL OF HAEMATOLOGY
    41. Bruno, C; Martinuzzi, A; Tang, YY; Andreu, AL; Pallotti, F; Bonilla, E; Shanske, S; Fu, J; Sue, CM; Angelini, C; DiMauro, S; Manfredi, G
      A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV

      AMERICAN JOURNAL OF HUMAN GENETICS
    42. SHIMADA Y; OKUNO S; KAWAI A; SHINOMIYA H; SAITO A; SUZUKI M; OMORI Y; NISHINO N; KANEMOTO N; FUJIWARA T; HORIE M; TAKAHASHI E
      CLONING AND CHROMOSOMAL MAPPING OF A NOVEL ABC TRANSPORTER GENE (HABC7), A CANDIDATE FOR X-LINKED SIDEROBLASTIC ANEMIA WITH SPINOCEREBELLARATAXIA

      JOURNAL OF HUMAN GENETICS
    43. Artik, S; Miller, A; Bretschneider, P; Schurer, N; Ruzicka, T
      Leg ulcers associated with sideroblastic anemia

      DERMATOLOGY
    44. YOSHIDA Y; OGUMA S; TOHYAMA K; UCHINO H; ITO M; TAKEDA Y; YOSHINAGA N; TASHIMA M; SAWADA H; OKUMA M
      DIAGNOSTIC AND BIOLOGICAL SIGNIFICANCE OF SIDEROBLASTIC ERYTHROPOIESIS IN THE MYELODYSPLASTIC SYNDROMES

      International journal of hematology
    45. EDGAR AJ; VIDYATILAKE HMS; WICKRAMASINGHE SN
      X-LINKED SIDEROBLASTIC ANEMIA DUE TO A MUTATION IN THE ERYTHROID 5-AMINOLEVULINATE SYNTHASE GENE LEADING TO AN ARGININE(170) TO LEUCINE SUBSTITUTION

      European journal of haematology
    46. BALDUINI CL; GUARNONE R; PECCI A; CENTENARA E; ASCARI F
      MULTILINEAGE DYSPLASIA WITHOUT INCREASED BLASTS IDENTIFIES A POOR-PROGNOSIS SUBSET OF MYELODYSPLASTIC SYNDROMES

      Leukemia
    47. TURLIN B; DEUGNIER Y
      EVALUATION AND INTERPRETATION OF IRON IN THE LIVER

      Seminars in diagnostic pathology
    48. MOORE MR
      THE BIOCHEMISTRY OF HEME-SYNTHESIS IN PORPHYRIA AND IN THE PORPHYRINURIAS

      Clinics in dermatology
    49. SANZ GF; SANZ MA; GREENBERG PL
      PROGNOSTIC FACTORS AND SCORING SYSTEMS IN MYELODYSPLASTIC SYNDROMES

      Haematologica
    50. VALLESPI T; IMBERT M; MECUCCI C; PREUDHOMME C; FENAUX P
      DIAGNOSIS, CLASSIFICATION, AND CYTOGENETICS OF MYELODYSPLASTIC SYNDROMES

      Haematologica
    51. MAY A; BISHOP DF
      THE MOLECULAR-BIOLOGY AND PYRIDOXINE RESPONSIVENESS OF X-LINKED SIDEROBLASTIC ANEMIA

      Haematologica
    52. MIJOVIC A; MUFTI GJ
      THE MYELODYSPLASTIC SYNDROMES - TOWARDS A FUNCTIONAL CLASSIFICATION

      Blood reviews
    53. BOTTOMLEY SS
      SECONDARY IRON OVERLOAD DISORDERS

      Seminars in hematology
    54. ZAK P; CHROBAK L; PODZIMEK K; PLISKOVA L; DEDIC K
      DYSERYTHROPOIETIC CHANGES AND SIDEROBLASTIC ANEMIA IN PATIENTS WITH HAIRY-CELL LEUKEMIA BEFORE AND AFTER THERAPY WITH 2-CHLORODEOXYADENOSINE

      Neoplasma
    55. SURINYA KH; COX TC; MAY BK
      IDENTIFICATION AND CHARACTERIZATION OF A CONSERVED ERYTHROID-SPECIFICENHANCER LOCATED IN INTRON-8 OF THE HUMAN 5-AMINOLEVULINATE SYNTHASE-2 GENE

      The Journal of biological chemistry
    56. Csere, P; Lill, R; Kispal, G
      Identification of a human mitochondrial ABC transporter, the functional orthologue of yeast Atm1p

      FEBS LETTERS
    57. BROKER S; MEUNIER B; RICH P; GATTERMANN N; HOFHAUS G
      MTDNA MUTATIONS ASSOCIATED WITH SIDEROBLASTIC ANEMIA CAUSE A DEFECT OF MITOCHONDRIAL CYTOCHROME-C-OXIDASE

      European journal of biochemistry
    58. TOTH T; BOKAY J; SZONYI L; NAGY B; PAPP Z
      DETECTION OF MTDNA DELETION IN PEARSON-SYNDROME BY 2 INDEPENDENT PCR ASSAYS FROM GUTHRIE CARD

      Clinical genetics
    59. EDGAR AJ; WICKRAMASINGHE SN
      HEREDITARY SIDEROBLASTIC ANEMIA DUE TO A MUTATION IN EXON-10 OF THE ERYTHROID 5-AMINOLEVULINATE SYNTHASE GENE

      British Journal of Haematology
    60. Furuyama, K; Uno, R; Urabe, A; Hayashi, N; Fujita, H; Kondo, M; Sassa, S; Yamamoto, M
      R411C mutation of the ALAS2 gene encodes a pyridoxine-responsive enzyme with low activity

      BRITISH JOURNAL OF HAEMATOLOGY
    61. HARIGAE H; SUWABE N; WEINSTOCK PH; NAGAI M; FUJITA H; YAMAMOTO M; SASSA S
      DEFICIENT HEME AND GLOBIN-SYNTHESIS IN EMBRYONIC STEM-CELLS LACKING THE ERYTHROID-SPECIFIC DELTA-AMINOLEVULINATE SYNTHASE GENE

      Blood
    62. SANZ GF; SANZ MA; VALLESPI T
      ETIOPATHOLOGY, PROGNOSIS AND THERAPY OF MYELODYSPLASTIC SYNDROMES

      HEMATOLOGY AND CELL THERAPY
    63. SCHULTZE AE; SCHAEFFER DO; POTTER MD; JOHNSON DK
      ALTERATIONS IN GROWTH, HEMATOPOIESIS AND SERUM CHEMISTRY PROFILES IN FITNESS 1(4226SB) MUTANT MICE

      Comparative haematology international
    64. GOEDSEELS J; DECALUWE JP; ALEXANDER M
      CONGENITAL SIDEROBLASTIC ANEMIA IN AN INFANT

      Archives de pediatrie
    65. LOWENTHAL RM; MARSDEN KA
      MYELODYSPLASTIC SYNDROMES

      International journal of hematology
    66. EDGAR AJ; LOSOWSKY MS; NOBLE JS; WICKRAMASINGHE SN
      IDENTIFICATION OF AN ARGININE(452) TO HISTIDINE SUBSTITUTION IN THE ERYTHROID 5-AMINOLEVULINATE SYNTHETASE GENE IN A LARGE PEDIGREE WITH X-LINKED HEREDITARY SIDEROBLASTIC ANEMIA

      European journal of haematology
    67. MIELOT F; BADERMEUNIER B; TCHERNIA G; DOMMERGUES JP
      MYELODYSPLASIA AND MITOCHONDRIAL CYTOPATHIES IN CHILDHOOD

      Pathologie et biologie
    68. PHATAK PD; JANAS JS; KOUIDES PA; SHAM RL; MARDER VJ
      UNUSUAL ANEMIAS

      American journal of hematology
    69. ABRUZZESE E; RAO PN; SLATKOFF M; CRUZ J; POWELL BL; JACKLE B; PETTENATI MJ
      MONOSOMY-X AS A RECURRING SOLE CYTOGENETIC ABNORMALITY ASSOCIATED WITH MYELODYSPLASTIC DISEASES

      Cancer genetics and cytogenetics
    70. MURAKI K; GOTO Y; NISHINO I; HAYASHIDANI M; TAKEUCHI S; HORAI S; SAKURA N; UEDA K
      SEVERE LACTIC-ACIDOSIS AND NEONATAL DEATH IN PEARSON SYNDROME

      Journal of inherited metabolic disease
    71. FUJITA H
      MOLECULAR MECHANISM OF HEME-BIOSYNTHESIS

      Tohoku Journal of Experimental Medicine
    72. SURINYA KH; COX TC; MAY BK
      TRANSCRIPTIONAL REGULATION OF THE HUMAN ERYTHROID 5-AMINOLEVULINATE SYNTHASE GENE - IDENTIFICATION OF PROMOTER ELEMENTS AND ROLE OF REGULATORY PROTEINS

      The Journal of biological chemistry
    73. NAGAI T; HARIGAE H; FURUYAMA K; MUNAKATA H; HAYASHI N; ENDO K; SASSA S; YAMAMOTO M
      5-AMINOLEVULINATE SYNTHASE EXPRESSION AND HEMOGLOBIN-SYNTHESIS IN A HUMAN MYELOGENOUS LEUKEMIA-CELL LINE

      Journal of Biochemistry
    74. SENECA S; DEMEIRLEIR L; DESCHEPPER J; BALDUCK N; JOCHMANS K; LIEBAERS I; LISSENS W
      PEARSON MARROW PANCREAS SYNDROME - A MOLECULAR STUDY AND CLINICAL MANAGEMENT

      Clinical genetics
    75. TUCKFIELD A; RATNAIKE S; HUSSEIN S; METZ J
      A NOVEL FORM OF HEREDITARY SIDEROBLASTIC ANEMIA WITH MACROCYTOSIS

      British Journal of Haematology
    76. TCHERNIA G; BADERMEUNIER B; LAVERGNE JM; MIELOT F; DOMMERGUES JP
      MYELODYSPLASIA IN CHILDHOOD MAY BE A POLYCLONAL DISEASE

      HEMATOLOGY AND CELL THERAPY
    77. PERRY AR; PAGLIUCA A; FITZSIMONS EJ; MUFTI GJ; WILLIAMS R
      ACQUIRED SIDEROBLASTIC ANEMIA INDUCED BY A COPPER-CHELATING AGENT

      International journal of hematology
    78. ESCUDIER SM; ALBITAR M; ROBERTSON LE; ANDREEFF M; PIERCE S; KANTARJIAN HM
      ACUTE LYMPHOBLASTIC-LEUKEMIA FOLLOWING PRELEUKEMIC SYNDROMES IN ADULTS

      Leukemia
    79. ROSATI S; MICK R; XU F; STONYS E; LEBEAU MM; LARSON R; VARDIMAN JW
      REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA - FURTHER CHARACTERIZATION OF AN UNCLASSIFIABLE MYELODYSPLASTIC SYNDROME

      Leukemia
    80. ILLARIOSHKIN SN; TANAKA H; MARKOVA ED; NIKOLSKAYA NN; IVANOVASMOLENSKAYA IA; TSUJI S
      X-LINKED NONPROGRESSIVE CONGENITAL CEREBELLAR HYPOPLASIA - CLINICAL DESCRIPTION AND MAPPING TO CHROMOSOME XQ

      Annals of neurology
    81. SABA HI
      MYELODYSPLASTIC SYNDROMES IN THE ELDERLY - THE ROLE OF GROWTH-FACTORSIN MANAGEMENT

      Leukemia research
    82. KARDOS G; VEERMAN AJP; DEWAAL FC; VANOUDHEUSDEN LJ; SLATER R
      FAMILIAL SIDEROBLASTIC ANEMIA WITH EMERGENCE OF MONOSOMY-5 AND MYELODYSPLASTIC SYNDROME

      Medical and pediatric oncology
    83. KAWAMURA S; YOSHIOKA T; KATO T; MATSUO M; YASUDA M
      HISTOLOGICAL-CHANGES IN RAT EMBRYONIC BLOOD-CELLS AS A POSSIBLE MECHANISM FOR VENTRICULAR SEPTAL-DEFECTS PRODUCED BY AN N-PHENYLIMIDE HERBICIDE

      Teratology
    84. KOUIDES PA; BENNETT JM
      MORPHOLOGY AND CLASSIFICATION OF THE MYELODYSPLASTIC SYNDROMES AND THEIR PATHOLOGICAL VARIANTS

      Seminars in hematology
    85. ROSATI S; ANASTASI J; VARDIMAN J
      RECURRING DIAGNOSTIC PROBLEMS IN THE PATHOLOGY OF THE MYELODYSPLASTICSYNDROMES

      Seminars in hematology
    86. HAMBLIN TJ
      IMMUNOLOGICAL ABNORMALITIES IN MYELODYSPLASTIC SYNDROMES

      Seminars in hematology
    87. LERNER A; BRANSKI D; LEBENTHAL E
      PANCREATIC DISEASES IN CHILDREN

      The Pediatric clinics of North America
    88. GATTERMANN N; RETZLAFF S; WANG YL; BERNEBURG M; HEINISCH J; WLASCHEK M; AUL C; SCHNEIDER W
      A HETEROPLASMIC POINT MUTATION OF MITOCHONDRIAL TRNA(LEU)(CUN) IN NONLYMPHOID HEMATOPOIETIC-CELL LINEAGES FROM A PATIENT WITH ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA

      British Journal of Haematology
    89. GATTERMANN N; BERNEBURG M; HEINISCH J; AUL C; SCHNEIDER W
      DETECTION OF THE AGING-ASSOCIATED 5-KB COMMON DELETION OF MITOCHONDRIAL-DNA IN BLOOD AND BONE-MARROW OF HEMATOLOGICALLY NORMAL ADULTS - ABSENCE OF THE DELETION IN CLONAL BONE-MARROW DISORDERS

      Leukemia
    90. KOUIDES PA; BENNETT JM
      TRANSFORMATION OF CHRONIC MYELOMONOCYTIC LEUKEMIA TO ACUTE LYMPHOBLASTIC-LEUKEMIA - CASE-REPORT AND REVIEW OF THE LITERATURE OF LYMPHOBLASTIC TRANSFORMATION OF MYELODYSPLASTIC SYNDROME

      American journal of hematology
    91. BLOK RB; THORBURN DR; THOMPSON GN; DAHL HHM
      A TOPOISOMERASE-II CLEAVAGE SITE IS ASSOCIATED WITH A NOVEL MITOCHONDRIAL-DNA DELETION

      Human genetics
    92. HANSON B; SZTERN B; VAMOS E; LUSTMAN F
      PHOSPHATURIA, GLYCOSURIA AND AMINOACIDURIA ASSOCIATED WITH IDIOPATHICACQUIRED SIDEROBLASTIC ANEMIA

      Clinical nephrology
    93. COTTER PD; DRABKIN HA; VARKONY T; SMITH DI; BISHOP DF
      ASSIGNMENT OF THE HUMAN HOUSEKEEPING DELTA-AMINOLEVULINATE SYNTHASE GENE (ALAS1) TO CHROMOSOME BAND 3P21.1 BY PCR ANALYSIS OF SOMATIC-CELL HYBRIDS

      Cytogenetics and cell genetics
    94. BOTTOMLEY SS; MAY BK; COX TC; COTTER PD; BISHOP DF
      MOLECULAR DEFECTS OF ERYTHROID 5-AMINOLEVULINATE SYNTHASE IN X-LINKEDSIDEROBLASTIC ANEMIA

      Journal of bioenergetics and biomembranes
    95. FORSYTH P; DAVIES JM
      PURE WHITE CELL APLASIA AND HEALTH FOOD-PRODUCTS

      Postgraduate medical journal
    96. COTTER PD; MAY A; FITZSIMONS EJ; HOUSTON T; WOODCOCK BE; ALSABAH AI; WONG L; BISHOP DF
      LATE-ONSET X-LINKED SIDEROBLASTIC ANEMIA

      The Journal of clinical investigation
    97. MUTA K; KRANTZ SB
      INHIBITION OF HEME-SYNTHESIS INDUCES APOPTOSIS IN HUMAN ERYTHROID PROGENITOR CELLS

      Journal of cellular physiology
    98. DIERLAMM J; MICHAUX L; CRIEL A; WLODARSKA I; ZELLER W; LOUWAGIE A; MICHAUX JL; MECUCCI C; VANDENBERGHE H
      ISODICENTRIC (X)(Q13) IN HEMATOLOGICAL MALIGNANCIES - PRESENTATION OF5 NEW CASES, APPLICATION OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)AND REVIEW OF THE LITERATURE

      British Journal of Haematology
    99. SMITH OP; HANN IM; WOODWARD CE; BROCKINGTON M
      PEARSONS MARROW PANCREAS SYNDROME - HEMATOLOGICAL FEATURES ASSOCIATEDWITH DELETION AND DUPLICATION OF MITOCHONDRIAL-DNA

      British Journal of Haematology
    100. TAKEDA Y; SAWADA H; SAWAI H; TOIMATSUDA T; TASHIMA M; OKUMA M; WATANABE S; OHMORI S; KONDO M
      ACQUIRED HYPOCHROMIC AND MICROCYTIC SIDEROBLASTIC ANEMIA RESPONSIVE TO PYRIDOXINE WITH LOW VALUE OF FREE ERYTHROCYTE PROTOPORPHYRIN - A POSSIBLE SUBGROUP OF IDIOPATHIC ACQUIRED SIDEROBLASTIC ANEMIA (IASA)

      British Journal of Haematology


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Documento generato il 05/08/20 alle ore 10:39:12