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    1. Zanella, A; Bianchi, P; Iurlo, A; Boschetti, C; Taioli, E; Vercellati, C; Zappa, M; Fermo, E; Tavazzi, D; Sampietro, M
      Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: Study of Italian cases

      BLOOD CELLS MOLECULES AND DISEASES
    2. Reinhardt, D; Witt, O; Miosge, N; Herken, R; Pekrun, A
      Increase in band 3 density and aggregation in hereditary spherocytosis

      BLOOD CELLS MOLECULES AND DISEASES
    3. Reinhardt, D; Witt, O; Miosge, N; Herken, R; Pekrun, A
      Increase in band 3 density and aggregation in hereditary spherocytosis

      BLOOD CELLS MOLECULES AND DISEASES
    4. Low, PS; Zhang, D; Bolin, JT
      Localization of mutations leading to altered cell shape and anion transport in the crystal structure of the cytoplasmic domain of band 3

      BLOOD CELLS MOLECULES AND DISEASES
    5. Hou, VC; Conboy, JG
      Regulation of alternative pre-mRNA splicing during erythroid differentiation

      CURRENT OPINION IN HEMATOLOGY
    6. Chui, DHK; Dover, GJ
      Sickle cell disease: no longer a single gene disorder

      CURRENT OPINION IN PEDIATRICS
    7. Hagerstrand, H; Iglic, A; Bobrowska-Hagerstrand, M; Lindqvist, C; Isomaa, B; Eber, S
      Amphiphile-induced vesiculation in aged hereditary spherocytosis erythrocytes indicates normal membrane stability properties under non-starving conditions

      MOLECULAR MEMBRANE BIOLOGY
    8. Corrons, JLV; Besson, I
      Red cell membrane Na+ transport systems in hereditary spherocytosis: relevance to understanding the increased Na+ permeability

      ANNALS OF HEMATOLOGY
    9. Xiros, N; Economopoulos, T; Papageorgiou, E; Mantzios, G; Raptis, S
      Massive hemothorax due to intrathoracic extramedullary hematopoiesis in a patient with hereditary spherocytosis

      ANNALS OF HEMATOLOGY
    10. de Lagausie, P; Rorlich, P; Benkerrou, M; Roessingh, AD; Malbezin, S; El Ghoneimi, A; Aigrain, Y
      Pediatric laparoscopic splenectomy: our experience and technique

      ARCHIVES DE PEDIATRIE
    11. Nakanishi, H; Kanzaki, A; Yawata, A; Yamada, O; Yawata, Y
      Ankyrin gene mutations in Japanese patients with hereditary spherocytosis

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    12. Tsomi, K; Karagiorga-Lagana, M; Karabatsos, F; Fragodimitri, C; van Vliet-Konstantinidou, C; Premetis, E; Stamoulakatou, A
      Arterial elastorrhexis in beta-thalassaemia intermedia, sickle cell thalassaemia and hereditary spherocytosis

      EUROPEAN JOURNAL OF HAEMATOLOGY
    13. Tokunaga, Y; Ohga, S; Suita, S; Matsushima, T; Hara, T
      Moyamoya syndrome with spherocytosis: Effect of splenectomy on strokes

      PEDIATRIC NEUROLOGY
    14. Perrotta, S; del Giudice, EM; Iolascon, A; De Vivo, M; Di Pinto, D; Cutillo, S; Nobili, B
      Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia

      LEUKEMIA
    15. Chou, R; DeLoughery, TG
      Recurrent thromboembolic disease following splenectomy for pyruvate kinasedeficiency

      AMERICAN JOURNAL OF HEMATOLOGY
    16. Eber, SW; Belohradsky, BH; Weiss, M
      Antiinfectious prophylaxis in asplenia.

      KLINISCHE PADIATRIE
    17. Granel, B; Serratrice, J; Rey, J; David, M; Pache, X; Bernit, E; Swiader, L; Disdier, P; Weiller, PJ
      Acute intra-familial erythroblastopenia and hereditary spherocytosis: roleof parvovirus B19 infection

      REVUE DE MEDECINE INTERNE
    18. Babaev, ES
      Mechanism of red cell destruction in inherited spherocytosis and approaches to elimination of the pathological process in children

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    19. Aleem, A; Murray, JA
      Spherocytosis preceding the development of myelodysplasia

      CLINICAL AND LABORATORY HAEMATOLOGY
    20. Danise, P; Amendola, G; Nobili, B; Perrotta, S; Del Giudice, EM; Matarese, SMR; Iolascon, A; Brugnara, C
      Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis

      CLINICAL AND LABORATORY HAEMATOLOGY
    21. Leung, KFS; Au, WY; Chan, AYY; Chan, LC; Waye, JS; Chui, DHK; Ma, SK
      Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family

      CLINICAL AND LABORATORY HAEMATOLOGY
    22. Aixala, MTF; Sarandria, CN
      Microspherocytosis. Relationship between erythroid profile and different laboratory tests.

      MEDICINA-BUENOS AIRES
    23. Williams, MW; Resneck, WG; Kaysser, T; Ursitti, JA; Birkenmeier, CS; Barker, JE; Bloch, RJ
      Na,K-ATPase in skeletal muscle: two populations of beta-spectrin control localization in the sarcolemma but not partitioning between the sarcolemma and the transverse tubules

      JOURNAL OF CELL SCIENCE
    24. Zhou, JZ; Low, PS
      Characterization of the reversible conformational equilibrium in the cytoplasmic domain of human erythrocyte membrane band 3

      JOURNAL OF BIOLOGICAL CHEMISTRY
    25. Chang, SH; Low, PS
      Regulation of the glycophorin C-protein 4.1 membrane-to-skeleton bridge and evaluation of its contribution to erythrocyte membrane stability

      JOURNAL OF BIOLOGICAL CHEMISTRY
    26. McCarty, JM
      Hereditary elliptocytosis

      LABORATORY MEDICINE
    27. Basseres, DS; Duarte, ASS; Hassoun, H; Costa, FF; Saad, STO
      beta-Spectrin S-ta Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism

      BRITISH JOURNAL OF HAEMATOLOGY
    28. Bracher, NA; Lyons, CA; Wessels, G; Mansvelt, E; Coetzer, TL
      Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III

      BRITISH JOURNAL OF HAEMATOLOGY
    29. Packman, CH
      The spherocytic haemolytic anaemias

      BRITISH JOURNAL OF HAEMATOLOGY
    30. del Giudice, EM; Nobili, B; Francese, M; D'Urso, L; Iolascon, A; Eber, S; Perrotta, S
      Clinical and molecular evaluation of non-dominant hereditary spherocytosis

      BRITISH JOURNAL OF HAEMATOLOGY
    31. Wandersee, NJ; Roesch, AN; Hamblen, NR; de Moes, J; van der Valk, MA; Bronson, RT; Gimm, JA; Mohandas, N; Demant, P; Barker, JE
      Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

      BLOOD
    32. Onoe, M; Magara, T; Yamamoto, Y
      Cardiac operation for a patient with autoimmune hemolytic anemia with warm-reactive antibodies

      ANNALS OF THORACIC SURGERY
    33. Bolton-Maggs, PHB
      The diagnosis and management of hereditary spherocytosis

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    34. F'ernandez-Alberti, A; Fink, NE
      Red blood cell osmotic fragility confidence intervals: a definition by application of a mathematical model

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    35. Quilty, JA; Reithmeier, RAF
      Trafficking and folding defects in hereditary spherocytosis mutants of thehuman red cell anion exchanger

      TRAFFIC
    36. Magni, P; Quaglini, S; Marchetti, M; Barosi, G
      Deciding when to intervene: a Markov decision process approach

      INTERNATIONAL JOURNAL OF MEDICAL INFORMATICS
    37. Degousee, N; Gupta, GD; Lew, RR; Heath, IB
      A putative spectrin-containing membrane skeleton in hyphal tips of Neurospora crassa

      FUNGAL GENETICS AND BIOLOGY
    38. Wandersee, NJ; Tait, JF; Barker, JE
      Erythroid phosphatidyl serine exposure is not predictive of thrombotic risk in mice with hemolytic anemia

      BLOOD CELLS MOLECULES AND DISEASES
    39. Shayakul, C; Alper, SL
      Inherited renal tubular acidosis

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    40. Shmukler, BE; Wilhelm, S; Alper, SL
      Short sequence repeat polymorphism in the mouse slc4al gene encoding the AE1.Cl-/HCO3- exchanger

      DNA SEQUENCE
    41. Lee, YK; Cho, HI; Park, SS; Lee, YJ; Ra, E; Chang, YH; Hur, M; Shin, HY; Ahn, HS
      Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis

      JOURNAL OF KOREAN MEDICAL SCIENCE
    42. Ghanayem, BI; Ward, SM; Chanas, B; Nyska, A
      Comparison of the acute hematotoxicity of 2-butoxyethanol in male and female F344 rats

      HUMAN & EXPERIMENTAL TOXICOLOGY
    43. Liao, EC; Paw, BH; Peters, LL; Zapata, A; Pratt, SJ; Do, CP; Lieschke, G; Zon, LI
      Hereditary spherocytosis in zebrafish riesling illustrates evolution of erythroid beta-spectrin structure, and function in red cell morphogenesis andmembrane stability

      DEVELOPMENT
    44. Park, A; Heniford, BT; Hebra, A; Fitzgerald, P
      Pediatric laparoscopic splenectomy

      SURGICAL ENDOSCOPY-ULTRASOUND AND INTERVENTIONAL TECHNIQUES
    45. Yawata, Y; Kanzaki, A; Yawata, A; Doerfler, W; Ozcan, R; Eber, SW
      Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    46. Yarali, N; Duru, F; Sipahi, T; Kara, A; Tezic, T
      Parvovirus B19 infection reminiscent of myelodysplastic syndrome in three children with chronic hemolytic anemia

      PEDIATRIC HEMATOLOGY AND ONCOLOGY
    47. Yazdanbakhsh, K; Lomas-Francis, C; Reid, ME
      Blood groups and diseases associated with inherited abnormalities of the red blood cell membrane

      TRANSFUSION MEDICINE REVIEWS
    48. Ricard, MP; Gilsanz, F; Millan, I
      Erythroid membrane protein defects in hereditary spherocytosis. A study of62 Spanish cases

      HAEMATOLOGICA
    49. Zarza, R; Moscardo, M; Alvarez, R; Garcia, J; Morey, M; Pujades, A; Vives-Corrons, JL
      Co-existence of hereditary spherocytosis and a new red cell pyruvate kinase variant: PK Mallorca

      HAEMATOLOGICA
    50. Beauchamp-Nicoud, A; Morle, L; Lutz, HU; Stammler, P; Agulles, O; Petermann-Khder, R; Iolascon, A; Perrotta, S; Cynober, T; Tchernia, G; Delaunay, J; Baudin-Creuza, V
      Heavy transfusions and presence of an anti-protein 4.2 antibody in 4.2(-) hereditary spherocytosis (949delG)

      HAEMATOLOGICA
    51. Murdock, RC; Reynolds, C; Sarelius, IH; Waugh, RE
      Adaptation and survival of surface-deprived red blood cells in mice

      AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
    52. Barker, JE; Deveau, S; Wandersee, NJ
      Amelioration of severe hereditary spherocytosis in nonablated adult mice by marrow transplantation

      EXPERIMENTAL HEMATOLOGY
    53. Dooner, GJ; Barker, JE; Gallagher, PG; Debatis, ME; Brown, AH; Forget, BG; Becker, PS
      Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro

      EXPERIMENTAL HEMATOLOGY
    54. Onodera, K; Shavit, JA; Motohashi, H; Yamamoto, M; Engel, JD
      Perinatal synthetic lethality and hematopoietic defects in compound mafG :mafK mutant mice

      EMBO JOURNAL
    55. Udden, MM
      Rat erythrocyte morphological changes after gavage dosing with 2-butoxyethanol: A comparison with the in vitro effects of butoxyacetic acid on rat and human erythrocytes

      JOURNAL OF APPLIED TOXICOLOGY
    56. Bertolotti, M; Loria, P; Martella, P; Carulli, L; De Santis, M; Carulli, N
      Bleeding jejunal varices and portal thrombosis in a splenectomized patientwith hereditary spherocytosis

      DIGESTIVE DISEASES AND SCIENCES
    57. Dhermy, D; Steen-Johnsen, J; Bournier, O; Hetet, G; Cynober, T; Tchernia, G; Grandchamp, B
      Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis family

      CLINICAL AND LABORATORY HAEMATOLOGY
    58. Ames, PRJ; Nardiello, S; Tommasino, C
      Efficacy of low dose intravenous immunoglobulins for post-splenectomy treatment of autoimmune haemolytic anaemia in a patient with hereditary spherocytosis

      CLINICAL AND LABORATORY HAEMATOLOGY
    59. Weatherall, DJ; Provan, AB
      Red cells I: inherited anaemias

      LANCET
    60. Moran, VP; del Cueto, ME; Delgado, NF; Damas, MS; Rivero, RV; Otero, AG; Barreras, PV; Svarch, E
      Effectiveness of the partial splenectomy in the treatment of hereditary spherocytosis.

      REVISTA DE INVESTIGACION CLINICA
    61. Sabatino, DE; Wong, C; Cline, AP; Pyle, L; Garrett, LJ; Gallagher, PG; Bodine, DM
      A minimal ankyrin promoter linked to a human gamma-globin gene demonstrates erythroid specific copy number dependent expression with minimal positionor enhancer dependence in transgenic mice

      JOURNAL OF BIOLOGICAL CHEMISTRY
    62. Roder, C; Dienemann, H
      Extramedullary hematopoiesis as a differential diagnosis of mediastinal masses

      CHIRURG
    63. Gallagher, PG; Ferreira, JDS; Costa, FF; Saad, STO; Forget, BG
      A recurrent frameshift mutation of the ankyrin gene associated with severehereditary spherocytosis

      BRITISH JOURNAL OF HAEMATOLOGY
    64. King, MJ; Behrens, J; Rogers, C; Flynn, C; Greenwood, D; Chambers, K
      Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia

      BRITISH JOURNAL OF HAEMATOLOGY
    65. Zhang, DC; Kiyatkin, A; Bolin, JT; Low, PS
      Crystallographic structure and functional interpretation of the cytoplasmic domain of erythrocyte membrane band 3

      BLOOD
    66. Gallagher, PG; Romana, M; Tse, WT; Lux, SE; Forget, BG
      The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter

      BLOOD
    67. Bruce, LJ; Tanner, MJA
      Erythroid band 3 variants and disease

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    68. Sato, T; Ueda, D; Sakota, SI; Haseyama, K; Chiba, S; Kudoh, T
      Pancytopenia with hemophagocytosis secondary to parvovirus B19 infection in a family with hereditary spherocytosis

      PEDIATRICS INTERNATIONAL
    69. Chiron, M; Cynober, T; Mielot, F; Tchernia, G; Croisille, L
      The GEN.S: a fortuitous finding of a routine screening test for hereditaryspherocytosis

      HEMATOLOGY AND CELL THERAPY
    70. Caprotti, R; Franciosi, C; Romano, F; Codecasa, G; Musco, F; Motta, M; Uggeri, F
      Combined laparoscopic splenectomy and cholecystectomy for the treatment ofhereditary spherocytosis: Is it safe and effective?

      SURGICAL LAPAROSCOPY ENDOSCOPY & PERCUTANEOUS TECHNIQUES
    71. Dhermy, D; Bournier, O; Bourgeois, M; Grandchamp, B
      The red blood cell band 3 variant (band 3(Bicetrel): R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect

      MOLECULAR MEMBRANE BIOLOGY
    72. Iglauer, A; Reinhardt, D; Schroter, W; Pekrun, A
      Cryohemolysis test as a diagnostic tool for hereditary spherocytosis

      ANNALS OF HEMATOLOGY
    73. Eber, SW; Langendorfer, CM; Ditzig, M; Reinhardt, D; Stohr, G; Soldan, W; Schroter, W; Tchernia, G
      Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis: impact of insufficient antibody response to pneumococcal infection

      ANNALS OF HEMATOLOGY
    74. Giuliani, AL; Bigoni, B; Veronesi, M; Manservigi, R; Mischiati, C; Berti, G; Zavagli, G; Ricci, G
      Membrane protein pattern in hereditary spherocytosis in five subjects fromnorth-east Italy obtained by SDS-PAGE using N,N '-diallyltartardiamide

      EUROPEAN JOURNAL OF HAEMATOLOGY
    75. Perrotta, S; Iolascon, A; Polito, R; d'Urzo, G; Conte, ML; del Giudice, EM
      4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis

      HAEMATOLOGICA
    76. Barker, JE; Kaysser-Kranich, TM; Hamblen, N; Deveau, S
      Multiple high cell dose injections of normal marrow into newborn jaundicedmice dramatically prolong life despite transient repopulation

      EXPERIMENTAL HEMATOLOGY
    77. Taylor, CPF; Luckit, JK; Perry, DJ
      Inherited protein C deficiency, protein S deficiency and hyperhomocysteineaemia in a patient with hereditary spherocytosis

      CLINICAL AND LABORATORY HAEMATOLOGY
    78. Johnson, RM; Panchoosingh, H; Goyette, G; Ravindranath, Y
      Increased erythrocyte deformability in fetal erythropoiesis and in erythrocytes deficient in glucose-6-phosphate dehydrogenase and other glycolytic enzymes

      PEDIATRIC RESEARCH
    79. Sandler, A; Winkel, G; Kimura, M; Soper, R
      The role of prophylactic cholecystectomy during splenectomy in children with hereditary spherocytosis

      JOURNAL OF PEDIATRIC SURGERY
    80. McMullin, MF
      The molecular basis of disorders of the red cell membrane

      JOURNAL OF CLINICAL PATHOLOGY
    81. Peters, LL; Jindel, HK; Gwynn, B; Korsgren, C; John, KM; Lux, SE; Mohandas, N; Cohen, CM; Cho, MR; Golan, DE; Brugnara, C
      Mild spherocytosis and altered red cell ion transport in protein 4.2-null mice

      JOURNAL OF CLINICAL INVESTIGATION
    82. Coles, SE; Ho, MM; Chetty, MC; Nicolaou, A; Stewart, GW
      A variant of hereditary stomatocytosis with marked pseudohyperkalaemia

      BRITISH JOURNAL OF HAEMATOLOGY
    83. Tse, WT; Lux, SE
      Red blood cell membrane disorders

      BRITISH JOURNAL OF HAEMATOLOGY
    84. Allen, SJ; O'Donnell, A; Alexander, NDE; Mgone, CS; Peto, TEA; Clegg, JB; Alpers, MP; Weatherall, DJ
      Prevention of cerebral malaria in children in Papua New Guinea by southeast Asian ovalocytosis band 3

      AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE
    85. Gallagher, PG; Forget, BG
      Hematologically important mutations: Spectrin and ankyrin variants in hereditary spherocytosis

      BLOOD CELLS MOLECULES AND DISEASES
    86. MARCHETTI M; QUAGLINI S; BAROSI G
      PROPHYLACTIC SPLENECTOMY AND CHOLECYSTECTOMY IN MILD HEREDITARY SPHEROCYTOSIS - ANALYZING THE DECISION IN DIFFERENT CLINICAL SCENARIOS

      Journal of internal medicine
    87. UYSAL Z; YILDIRMAK Y; AKAR N; BASAK N; CIN S
      ALPHA-THALASSEMIA AND HEREDITARY SPHEROCYTOSIS IN THE SAME PATIENT - THE INTERACTION OF 2 DISEASES

      Pediatric hematology and oncology
    88. ZELINSKI T
      ERYTHROCYTE BAND-3 ANTIGENS AND THE DIEGO BLOOD-GROUP SYSTEM

      Transfusion medicine reviews
    89. Casey, JR; Reithmeier, RAF
      Anion exchangers in the red cell and beyond

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    90. BURSAUX E
      EXTENSIVE THROMBOSIS IN BAND3 NULL MICE

      MS. Medecine sciences
    91. PIPERNO A
      CLASSIFICATION AND DIAGNOSIS OF IRON OVERLOAD

      Haematologica
    92. DELGIUDICE EM; PERROTTA S; LOMBARDI C; IOLASCON A
      DECISION-MAKING AT THE BEDSIDE - DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A TRANSFUSED INFANT

      Haematologica
    93. IOLASCON A; DELGIUDICE EM; PERROTTA S; ALLOISIO N; MORLE L; DELAUNAY J
      HEREDITARY SPHEROCYTOSIS - FROM CLINICAL TO MOLECULAR DEFECTS

      Haematologica
    94. STREICHMAN S; GESCHEIDT Y
      CRYOHEMOLYSIS FOR THE DETECTION OF HEREDITARY SPHEROCYTOSIS - CORRELATION STUDIES WITH OSMOTIC FRAGILITY AND AUTOHEMOLYSIS

      American journal of hematology
    95. HAYETTE S; CARRE G; BOZON M; ALLOISIO N; MAILLET P; WILMOTTE R; PASCAL O; REYNAUD J; REMAN O; STEPHAN JL; MORLE L; DELAUNAY J
      2 DISTINCT TRUNCATED VARIANTS OF ANKYRIN ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS

      American journal of hematology
    96. HAYAGBARIN JE; SMITH RE; TUCKER FC
      HEREDITARY SPHEROCYTOSIS, THROMBOCYTOSIS, AND CHRONIC PULMONARY EMBOLI - A CASE-REPORT AND REVIEW OF THE LITERATURE

      American journal of hematology
    97. PETROF BJ
      THE MOLECULAR-BASIS OF ACTIVITY-INDUCED MUSCLE INJURY IN DUCHENNE MUSCULAR-DYSTROPHY

      Molecular and cellular biochemistry
    98. MGONE CS; GENTON B; PETER W; PANIU MM; ALPERS MP
      THE CORRELATION BETWEEN MICROSCOPIC EXAMINATION AND ERYTHROCYTE BAND-3 (AE1) GENE DELETION IN SOUTH-EAST ASIAN OVALOCYTOSIS

      Transactions of the Royal Society of Tropical Medicine and Hygiene
    99. KARET FE; GAINZA FJ; GYORY AZ; UNWIN RJ; WRONG O; TANNER MJA; NAYIR A; ALPAY H; SANTOS F; HULTON SA; BAKKALOGLU A; OZEN S; CUNNINGHAM MJ; DIPIETRO A; WALKER WG; LIFTON RP
      MUTATIONS IN THE CHLORIDE-BICARBONATE EXCHANGER GENE AE1 CAUSE AUTOSOMAL-DOMINANT BUT NOT AUTOSOMAL RECESSIVE DISTAL RENAL TUBULAR-ACIDOSIS

      Proceedings of the National Academy of Sciences of the United Statesof America
    100. Tanphaichitr, VS; Sumboonnanonda, A; Ideguchi, H; Shayakul, C; Brugnara, C; Takao, M; Veerakul, G; Alper, SL
      Novel AE1 mutations in recessive distal renal tubular acidosis - Loss-of-function is rescued by glycophorin A

      JOURNAL OF CLINICAL INVESTIGATION


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Documento generato il 11/08/20 alle ore 06:37:01