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La ricerca find articoli where soggetti phrase all words 'HEMOPHILIA-A' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 845 riferimenti
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    1. Liu, P; Kalajzic, I; Stover, ML; Rowe, DW; Lichtler, AC
      Human bone marrow stromal cells are efficiently transduced by vesicular stomatitis virus-pseudotyped retrovectors without affecting subsequent osteoblastic differentiation

      BONE
    2. Stein, CS; Kang, Y; Sauter, SL; Townsend, K; Staber, P; Derksen, TA; Martins, I; Qian, J; Davidson, BL; McCray, PB
      In vivo treatment of hemophilia A and mucopolysaccharidosis type VII usingnonprimate lentiviral vectors

      MOLECULAR THERAPY
    3. McCormack, JE; Edwards, W; Sensintaffer, J; Lillegren, L; Kozloski, M; Brumm, D; Karavodin, L; Jolly, DJ; Greengard, J
      Factors affecting long-term expression of a secreted transgene product after intravenous administration of a retroviral vector

      MOLECULAR THERAPY
    4. Mazurier, C; Goudemand, J; Hilbert, L; Caron, C; Fressinaud, E; Meyer, D
      Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    5. Kouides, PA
      Obstetric and gynaecological aspects of von Willebrand disease

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    6. Minhas, HL; Giangrande, PLF
      Presentation of severe haemophilia - A role for accident and emergency doctors?

      EMERGENCY MEDICINE JOURNAL
    7. Emanuel, BS; Shaikh, TH
      Segmental duplications: An 'expanding' role in genomic instability and disease

      NATURE REVIEWS GENETICS
    8. Pflegerl, K; Hahn, R; Schallaun, E; Josic, D; Jungbauer, A
      Quantification of plasma-derived blood coagulation factor VIII by real-time biosensor measurements

      JOURNAL OF CHROMATOGRAPHY B
    9. Fischer, K; Van der Bom, JG; Mauser-Bunschoten, EP; Roosendaal, G; Prejs, R; Grobbee, DE; Van den Berg, HM
      Changes in treatment strategies for severe haemophilia over the last 3 decades: effects on clotting factor consumption and arthropathy

      HAEMOPHILIA
    10. Timur, AA; Gurgey, A; Aktuglu, G; Kavakli, K; Canatan, D; Olek, K; Caglayan, SH
      Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations

      HAEMOPHILIA
    11. Gilchrist, GS; Wilke, JL; Muehlenbein, LR; Danilenko-Dixon, D
      Intrauterine correction of factor VIII (FVIII) deficiency

      HAEMOPHILIA
    12. Vianello, F; Belvini, D; Dal Bello, F; Tagariello, G; Zanon, E; Lombardi, AM; Zerbinati, P; Girolami, A
      Mild bleeding diathesis in a boy with combined severe haemophilia B (C-10400 -> T) and heterozygous factor V Leiden

      HAEMOPHILIA
    13. Cooper, HA; Jones, CP; Campion, E; Roberts, HR; Hedner, U
      Rationale for the use of high dose rFVIIa in a high-titre inhibitor patient with haemophilia B during major orthopaedic procedures

      HAEMOPHILIA
    14. Scharrer, I; Ehrlich, HJ
      Lack of evidence for increased inhibitor incidence in patients switched from plasma-derived to recombinant factor VIII

      HAEMOPHILIA
    15. Mauser-Bunschoten, EP; van der Bom, JG; Bongers, M; Twijnstra, M; Roosendaal, G; Fischer, K; van den Berg, HM
      Purity of factor VIII product and incidence of inhibitors in previously untreated patients with haemophilia A

      HAEMOPHILIA
    16. Theophilus, BDM; Enayat, MS; Williams, MD; Hill, FGH
      Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A

      HAEMOPHILIA
    17. Acquila, M; Bottini, F; Valetto, A; Caprino, D; Mori, PG; Bicocchi, MP
      A new strategy for prenatal diagnosis in a sporadic haemophilia B family

      HAEMOPHILIA
    18. Bauduer, F; Ducout, L; Bendriss, P; Falaises, B; Lavergne, JM
      Mild haemophilia A discovered in a previously multi-operated 73-year-old man: characterization of a new mutation

      HAEMOPHILIA
    19. Yoshioka, A; Shima, M; Fukutake, K; Takamatsu, J; Shirahata, A
      Safety and efficacy of a new recombinant FVIII formulated with sucrose (rFVIII-FS) in patients with haemophilia A: a long-term, multicentre clinical study in Japan

      HAEMOPHILIA
    20. Leissinger, C; Becton, D; Cornell, C; Gill, JC
      High-dose DDAVP intranasal spray (Stimate((R))) for the prevention and treatment of bleeding in patients with mild haemophilia A, mild or moderate type 1 von Willebrand disease and symptomatic carriers of haemophilia A

      HAEMOPHILIA
    21. Astermark, J; Berntorp, E; White, GC; Kroner, BL
      The Malmo International Brother Study (MIBS): further support for genetic predisposition to inhibitor development

      HAEMOPHILIA
    22. Ghosh, K; Shetty, S; Kulkarni, B; Nair, S; Pawar, A; Khare, A; Baindur, S; Mohanty, D
      Development of inhibitors in patients with haemophilia from India

      HAEMOPHILIA
    23. Schoenmakers, MAGC; Gulmans, VAM; Helders, PJM; Van den Berg, HM
      Motor performance and disability in Dutch children with haemophilia: a comparison with their healthy peers

      HAEMOPHILIA
    24. Soares, RPS; Chamone, DAF; Bydlowski, SP
      Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis

      HAEMOPHILIA
    25. Klein, I; Andrikovics, H; Bors, A; Nemes, L; Tordai, A; Varadi, A
      A haemophilia A and B molecular genetic diagnostic programme in Hungary: ahighly informative and cost-effective strategy

      HAEMOPHILIA
    26. Faradji, A; Bonnomet, F; Lecocq, J; Grunebaum, L; Desprez, D; Kern, O; Barbier, L; Sibilia, J
      Knee joint arthroplasty in a patient with haemophilia A and high inhibitortitre using recombinant factor VIIa (NovoSeven((R))): a new case report and review of the literature

      HAEMOPHILIA
    27. Yenchitsomanus, P; Thanootarakul, P; Akkarapatumwong, V; Oranwiroon, S; Pung-Amritt, P; Veerakul, G; Mahasandana, C
      Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection

      HAEMOPHILIA
    28. Philipp, CS
      Viral safety of a pasteurized, monoclonal antibody-purified factor VIII concentrate in previously untreated haemophilia A patients

      HAEMOPHILIA
    29. Haya, S; Lopez, MF; Aznar, JA; Batlle, J
      Immune tolerance treatment in haemophilia patients with inhibitors: the Spanish Registry

      HAEMOPHILIA
    30. Grunewald, M; Beneke, H; Guthner, C; Germowitz, A; Brommer, A; Griesshammer, M
      Acquired haemophilia: experiences with a standardized approach

      HAEMOPHILIA
    31. Puetz, JJ; Bouhasin, JD
      High-titre factor VIII inhibitor in two children with mild haemophilia A

      HAEMOPHILIA
    32. Sheth, S; DiMichele, D; Lee, M; Lamour, J; Quaegebeur, J; Hsu, D; Addonizio, L; Piomelli, S
      Heart transplant in a factor VIII-deficient patient with a high-titre inhibitor: perioperative management using high-dose continuous infusion factor VIII and recombinant factor VIIa

      HAEMOPHILIA
    33. Ghosh, K; Shetty, S; Mohanty, D
      Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay

      HAEMOPHILIA
    34. Mondorf, W; Klinge, J; Luban, NLC; Bray, G; Saenko, E; Scandella, D
      Low factor VIII recovery in haemophilia A patients without inhibitor titreis not due to the presence of anti-factor VIII antibodies undetectable by the Bethesda assay

      HAEMOPHILIA
    35. Oranwiroon, S; Akkarapatumwong, V; Pung-Amritt, P; Treesucon, A; Veerakul, G; Mahasandana, C; Panyim, S; Yenchitsomanus, P
      Determination of haemophilia A carrier status by mutation analysis

      HAEMOPHILIA
    36. Klinge, J; Auerswald, G; Budde, U; Klose, H; Kreuz, W; Lenk, H; Scandella, D
      Detection of all anti-factor VIII antibodies in haemophilia A patients by the Bethesda assay and a more sensitive immunoprecipitation assay

      HAEMOPHILIA
    37. Rocino, A; Papa, ML; Salerno, E; Capasso, F; Miraglia, E; De Biasi, R
      Immune tolerance induction in haemophilia A patients with high-responding inhibitors to factor VIII: experience at a single institution

      HAEMOPHILIA
    38. Calvez, T; Biou, M; Costagliola, D; Jullien, AM; Laurian, Y; Rossi, F; Rothschild, C; Sie, P
      The French haemophilia cohort: rationale and organization of a long-term national pharmacosurveillance system

      HAEMOPHILIA
    39. Miller, R
      The responsibility of separating truth from myth to patient and family

      HAEMOPHILIA
    40. Mauser-Bunschoten, EP; Roosendaal, G; Van den Berg, HM
      Product choice and haemophilia treatment in the Netherlands

      HAEMOPHILIA
    41. Penner, JA
      Haemophilic patients with inhibitors to factor VIII or IX: variables affecting treatment response

      HAEMOPHILIA
    42. Berntorp, E
      Immune tolerance induction: recombinant vs. human-derived product

      HAEMOPHILIA
    43. Aledort, LM
      Making a therapeutic choice: human versus recombinant fractions - can we do it?

      HAEMOPHILIA
    44. Ragni, MV
      New-generation recombinant factor concentrates: bridge to gene therapy

      HAEMOPHILIA
    45. Castro, RR; Relinque, NB; Alvarez, AC; Montes, JMG; Gutierrez, JMH
      Use of recombinant factor VII in Hepatology

      REVISTA ESPANOLA DE ENFERMEDADES DIGESTIVAS
    46. Turgeman, G; Pittman, DD; Muller, R; Kurkalli, BG; Zhou, SH; Pelled, G; Peyser, A; Zilberman, Y; Moutsatsos, IK; Gazit, D
      Engineered human mesenchymal stem cells: a novel platform for skeletal cell mediated gene therapy

      JOURNAL OF GENE MEDICINE
    47. Peterson, SR; Joseph, AK
      Inherited bleeding disorders, in dermatologic surgery

      DERMATOLOGIC SURGERY
    48. Poon, MC
      Use of recombinant factor VIIa in hereditary bleeding disorders

      CURRENT OPINION IN HEMATOLOGY
    49. Ananyeva, NM; Kouiavskaia, DV; Shima, M; Saenko, LL
      Catabolism of the coagulation factor VIII - Can we prolong lifetime of f VIII in circulation?

      TRENDS IN CARDIOVASCULAR MEDICINE
    50. Shetty, S; Ghosh, K; Bhide, A; Mohanty, D
      Carrier detection and prenatal diagnosis in families with haemophilia

      NATIONAL MEDICAL JOURNAL OF INDIA
    51. Aradhya, S; Bardaro, T; Galgoczy, P; Yamagata, T; Esposito, T; Patlan, H; Ciccodicola, A; Munnich, A; Kenwrick, S; Platzer, M; D'Urso, M; Nelson, DL
      Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes

      HUMAN MOLECULAR GENETICS
    52. Aradhya, S; Woffendin, H; Jakins, T; Bardaro, T; Esposito, T; Smahi, A; Shaw, C; Levy, M; Munnich, A; D'Urso, M; Lewis, RA; Kenwrick, S; Nelson, DL
      A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations

      HUMAN MOLECULAR GENETICS
    53. Smales, CM; Pepper, DS; James, DC
      Evaluation of protein modification during anti-viral heat bioprocessing byelectrospray ionization mass spectrometry

      RAPID COMMUNICATIONS IN MASS SPECTROMETRY
    54. Shwaiki, A; Lara, L; Ahmed, F; Crock, R; Rutecki, GW; Whittier, FC
      Acquired inhibitor to factor VIII in small cell lung cancer: a case reportand review of the literature

      ANNALS OF HEMATOLOGY
    55. Theodossiades, G; Tsevrenis, N; Nomikou, E; Dadiotis, L; Kontopoulou-Griva, I
      Surgery-associated acquired hemophilia A

      ANNALS OF HEMATOLOGY
    56. Sommer, SS; Scaringe, WA; Hill, KA
      Human germline mutation in the factor IX gene

      MUTATION RESEARCH-DNA REPAIR
    57. Fischer, G; Hoots, WK; Abrams, C
      Viral reduction techniques: Types and purpose

      TRANSFUSION MEDICINE REVIEWS
    58. Balabaud-Pichon, V; Freys, G; Faradji, A; Wolf, P; Pottecher, T
      Liver transplantation in a patient with haemophilia A and end stage liver failure

      ANNALES FRANCAISES D ANESTHESIE ET DE REANIMATION
    59. Berrettini, M; Mariani, G; Schiavoni, M; Rocino, A; Di Paolantonio, T; Longo, G; Morfini, M
      Pharmacokinetic evaluation of recombinant, activated factor VII in patients with inherited factor VII deficiency

      HAEMATOLOGICA
    60. Woods, AI; Meschengieser, SS; Blanco, AN; Salviu, MJ; Farias, CE; Kempfer, AC; Lazzari, MA
      Clinical features and laboratory patterns in a cohort of consecutive Argentinian patients with von Willebrand's disease

      HAEMATOLOGICA
    61. Casonato, A; Pontara, E; Sartorello, F; Gemmati, D; Cattini, MG; Girolami, A
      Combined hemophilia A and type 2N von Willebrand's disease: defect of bothfactor VIII level and factor VIII binding capacity of von Willebrand factor

      HAEMATOLOGICA
    62. Ewenstein, BM
      Continuous infusion of recombinant factor VIIa: Continue or not?

      THROMBOSIS AND HAEMOSTASIS
    63. Smith, MP; Ludlam, CA; Collins, PW; Hay, CRM; Wilde, JT; Grigeri, A; Melsen, T; Savidge, GF
      Elective surgery on factor VIII inhibitor patients using continuous infusion of recombinant activated factor VII - Plasma factor VII activity of 10 IU/ml is associated with an increased incidence of bleeding

      THROMBOSIS AND HAEMOSTASIS
    64. Santagostino, E; Morfini, M; Rocino, A; Baudo, F; Scaraggi, FA; Gringeri, A
      Relationship between factor VII activity and clinical efficacy of recombinant factor VIIa given by continuous infusion to patients with factor VIII inhibitors

      THROMBOSIS AND HAEMOSTASIS
    65. Mosnier, LO; Lisman, T; van den Berg, HM; Nieuwenhuis, HK; Meijers, JCM; Bouma, BN
      The defective down regulation of fibrinolysis in haemophilia A can be restored by increasing the TAFI plasma concentration

      THROMBOSIS AND HAEMOSTASIS
    66. Hollestelle, MJ; Thinnes, T; Crain, K; Stiko, A; Kruijt, JK; van Berkel, TJC; Loskutoff, DJ; van Mourik, JA
      Tissue distribution of factor VIII gene expression in vivo - A closer look

      THROMBOSIS AND HAEMOSTASIS
    67. Plantier, JL; Rodriguez, MH; Enjolras, N; Attali, O; Negrier, C
      A factor VIII minigene comprising the truncated intron I of factor IX highly improves the in vitro production of factor VIII

      THROMBOSIS AND HAEMOSTASIS
    68. Mannucci, PM
      Treatment of von Willebrand disease

      THROMBOSIS AND HAEMOSTASIS
    69. Oldenburg, J
      Mutation profiling in haemophilia A

      THROMBOSIS AND HAEMOSTASIS
    70. Vidal, F; Farssac, E; Altisent, C; Puig, L; Gallardo, D
      Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: Identification of 14 novel mutations

      THROMBOSIS AND HAEMOSTASIS
    71. Ettingshausen, CE; Halimeh, S; Kurnik, K; Schobess, R; Wermes, C; Junker, R; Kreuz, W; Pollmann, H; Nowak-Gottl, U
      Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors

      THROMBOSIS AND HAEMOSTASIS
    72. Lewis, DA; Moore, KD; Ortel, TL
      Factor VIII Arg2304 -> His binds to phosphatidylserine and is a functionalcofactor in the factor X-ase complex

      THROMBOSIS AND HAEMOSTASIS
    73. Bjorkman, S; Berntorp, E
      Pharmacokinetics of coagulation factors clinical relevance for patients with haemophilia

      CLINICAL PHARMACOKINETICS
    74. Lutze, G; Aumann, V; Lutze, G; Mittler, U
      Factor VIII inhibitors in patients suffering from severe haemophilla A: problems of "very low" responders

      KLINISCHE PADIATRIE
    75. Levesque, H; Borg, JY; Bossi, P; Goudemand, J; Guillet, B; Cabane, J
      Acquired haemophilia: diagnosis and therapeutic management.

      REVUE DE MEDECINE INTERNE
    76. Bishop, PR; Nowicki, MJ; Subramony, C; Parker, PH
      Solitary rectal ulcer - A rare cause of gastrointestinal bleeding in an adolescent with hemophilia A

      JOURNAL OF CLINICAL GASTROENTEROLOGY
    77. Fabricius, AM; Krueger, M; Falk, V; Hanke, M; Mohr, FW
      Floating thrombus on an ASD occluder device in a patient with hemophilia A

      THORACIC AND CARDIOVASCULAR SURGEON
    78. Oldenburg, J; Ivaskevicius, V; Rost, S; Fregin, A; White, K; Holinski-Feder, E; Muller, CR; Weber, BHF
      Evaluation of DHPLC in the analysis of hemophilia A

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    79. Astermark, J; Tengborn, L; Hedner, U; Berntorp, E
      Anti- and procoagulant activities in factor VII-deficient subjects

      THROMBOSIS RESEARCH
    80. Saenko, E; Josic, D; Stadler, M; Sarafanov, A; Lim, YP; Shima, M; Ananyeva, N; Schwinn, H
      Molecular modifications in factor VIII concentrates produced from different plasma pools

      THROMBOSIS RESEARCH
    81. Huang, CC; Li, LT; Shen, MC; Chen, JY; Lin, SW
      Domain specific monoclonal anti-factor VIII antibodies generated by inclusion body-renatured factor VIII peptides

      THROMBOSIS RESEARCH
    82. Prachalias, AA; Pozniak, A; Taylor, C; Srinivasan, P; Muiesan, P; Wendon, J; Cramp, M; Williams, R; O'Grady, J; Rela, M; Heaton, ND
      Liver transplantation in adults coinfected with HIV

      TRANSPLANTATION
    83. Poon, MC; d'Oiron, R; Hann, I; Negrier, C; de Lumley, L; Thomas, A; Karafoulidou, A; Demers, C; Street, A; Huth-Kuhne, A; Petrini, P; Fressinaud, E; Morfini, M; Tengborn, L; Marques-Verdier, A; Musso, R; Devecioglu, O; Houston, DS; Lethagen, S; Van Geet, C; von Depka, M; Berger, C; Beurrier, P; Britton, HA; Gerrits, W; Guthner, C; Kuhle, S; Lorenzo, JJ; Makris, PE; Nohe, N; Paugy, P; Pautard, B; Torchet, MF; Trillot, N; Vicariot, M; Wilde, J; Winter, M; Chambost, H; Ingerslev, J; Peters, M; Strauss, G
      Use of recombinant factor VIIa (NovoSeven (R)) in patients with Glanzmann thrombasthenia

      SEMINARS IN HEMATOLOGY
    84. Shapiro, A
      Inhibitor treatment: State of the art

      SEMINARS IN HEMATOLOGY
    85. Courter, SG; Bedrosian, CL
      Clinical evaluation of B-domain deleted recombinant factor VIII in previously treated patients

      SEMINARS IN HEMATOLOGY
    86. Courter, SG; Bedrosian, CL
      Clinical evaluation of B-domain deleted recombinant factor VIII in previously untreated patients

      SEMINARS IN HEMATOLOGY
    87. Fryer, JP; Oetting, WS; Brott, MJ; King, RA
      Alternative splicing of the tryrosinase gene transcript in normal human melanocytes and lymphocytes

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    88. Rechtine, GR; Bolesta, MJ; Chrin, AM; Louis, K
      Spontaneous resolution of symptomatic post-traumatic cervical epidural hematoma - A case report

      JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME
    89. Jacome, DE
      Idiopathic intracranial hypertension and hemophilia A

      HEADACHE
    90. Kawasaki, K; Minoshima, S; Nakato, E; Shibuya, K; Shintani, A; Asakawa, S; Sasaki, T; Klobeck, HG; Combriato, G; Zachau, HG; Shimizu, N
      Evolutionary dynamics of the human immunoglobulin kappa locus and the germline repertoire of the V kappa genes

      EUROPEAN JOURNAL OF IMMUNOLOGY
    91. Desai, UJ; Slosberg, ED; Boettcher, BR; Caplan, SL; Fanelli, B; Stephan, Z; Gunther, VJ; Kaleko, M; Connelly, S
      Phenotypic correction of diabetic mice by adenovirus-mediated glucokinase expression

      DIABETES
    92. High, KA
      Gene transfer as an approach to treating hemophilia

      CIRCULATION RESEARCH
    93. Kamphuisen, PW; Eikenboom, JCJ; Rosendaal, FR; Koster, T; Blann, AD; Vos, HL; Bertina, RM
      High factor VIII antigen levels increase the risk of venous thrombosis butare not associated with polymorphisms in the von Willebrand factor and factor VIII gene

      BRITISH JOURNAL OF HAEMATOLOGY
    94. Ling, M; Duncan, EM; Rodgers, SE; Somogyi, AA; Crabb, GA; Street, AM; Lloyd, JV
      Classification of the kinetics of factor VIII inhibitors in haemophilia A:plasma dilution studies are more discriminatory than time-course studies

      BRITISH JOURNAL OF HAEMATOLOGY
    95. Kjalke, M; Ezban, M; Monroe, DM; Hoffman, M; Roberts, HR; Hedner, U
      High-dose factor VIIa increases initial thrombin generation and mediates faster platelet activation in thrombocytopenia-like conditions in a cell-based model system

      BRITISH JOURNAL OF HAEMATOLOGY
    96. Huang, CC; Shen, MC; Chen, JY; Hung, MH; Hsu, TC; Lin, SW
      Epitope mapping of factor VIII inhibitor antibodies of Chinese origin

      BRITISH JOURNAL OF HAEMATOLOGY
    97. Lorenzo, JI; Lopez, A; Altisent, C; Aznar, JA
      Incidence of factor VIII inhibitors in severe haemophilia: the importance of patient age

      BRITISH JOURNAL OF HAEMATOLOGY
    98. David, D; Saenko, EL; Santos, IMA; Johnson, DJD; Tuddenham, EGD; McVey, JH; Kemball-Cook, G
      Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM-) and G1948D (CRMr)

      BRITISH JOURNAL OF HAEMATOLOGY
    99. Ivaskevicius, V; Jurgutis, R; Rost, S; Muller, A; Schmitt, C; Wulff, K; Herrmann, FH; Muller, CR; Schwaab, R; Oldenburg, J
      Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data

      BRITISH JOURNAL OF HAEMATOLOGY
    100. Toyoda, H; Fukuda, Y; Yokozaki, S; Hayashi, K; Saito, H; Takamatsu, J
      Safety and complications of interventional radiology for hepatocellular carcinoma in patients with haemophilia and cirrhosis

      BRITISH JOURNAL OF HAEMATOLOGY


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Documento generato il 26/05/20 alle ore 06:24:10