Results 141 to 150 of about 743 (212)

Assessment of interleukin-10 promoter variant (-1082A/G) and cytokine production in patients with hemolytic uremic syndrome. [PDF]

Front Pediatr, 2023
Mongelos MA, Sosa FN, Pineda GE, Fiorentino G, Santiago A, Abelleyro MM, Rossetti LC, Exeni R, De Brasi CD, Palermo MS, Ramos MV.   +10 more
europepmc   +1 more source

Evaluación del tratamiento con implantes dentales en pacientes con hemofilia

Introducción: La hemofilia es un desorden hemorrágico congénito y hereditario recesivo, portado por mujeres y que afecta a varones. Esta enfermedad, caracterizada por el sangrado prolongado y o anormal, está originada por mutaciones en el cromosoma X y ...
Gatti, Patricio C.
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Long-Term Follow-Up of a Portuguese Single-Centre Cohort of Persons with Haemophilia and Hepatitis C Virus Infection. [PDF]

GE Port J Gastroenterol, 2021
Pereira Guedes T, Garrido M, Kuttner Magalhães R, Moreira T, Rocha M, Maia L, Manuel Ferreira J, Morais S, Pedroto I.   +8 more
europepmc   +1 more source

EVALUATION OF THE RADIOISOTOPIC SYNOVECTOMY PROTOCOL IN PATIENTS WITH HEMOPHILIA. [PDF]

Acta Ortop Bras
Martins MDS, Ricciardi JBDS, Santos AO, Ozelo MC, Pagnano RG, Sakuma ETI.   +5 more
europepmc   +1 more source

Assessment of Static Balance with and Without Cognitive Dual Task in Children with Haemophilia: A Cross-Sectional Study. [PDF]

J Funct Morphol Kinesiol
Chimeno-Hernández A, Alberola-Zorrilla P, Martín Campos J, Carrasco JJ, Pérez-Alenda S, Sánchez Zuriaga D, Aguilar-Rodríguez M.   +6 more
europepmc   +1 more source

F8/F9 variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation Project. [PDF]

Res Pract Thromb Haemost, 2023
Labarque V, Mancuso ME, Kartal-Kaess M, Ljung R, Mikkelsen TS, Andersson NG.   +5 more
europepmc   +1 more source

Co-inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction. [PDF]

Br J Haematol
Bandini P, Borràs N, Martin-Fernandez L, Fernández-Mosteirín N, Aguinaco MR, Benítez O, Comes N, Ramírez L, González N, Lera C, Altisent C, Vidal F, Corrales I.   +12 more
europepmc   +1 more source

Real-World Data on the Effectiveness and Safety of wilate for the Treatment of von Willebrand Disease. [PDF]

TH Open, 2021
Sholzberg M, Khair K, Yaish H, Rodgers G, Cruz MS, Mejía CM, Čermáková Z, Matino D, Teitel J, Barrie A, Werner S, Prondzinski MVD.   +11 more
europepmc   +1 more source

Surgical Excision of a Hemophilic Pseudotumor Causing Vascular Impingement in a Patient with Severe Hemophilia A: A Case Report. [PDF]

Rev Bras Ortop (Sao Paulo)
Pradilla JM, Tinoco A, Cely LM, Buitrago MP.   +3 more
europepmc   +1 more source

Hemofilia: uma breve revisão bibliográfica

O sangue é produzido na medula óssea dos ossos chatos, vértebras, costelas, quadril, crânio e esterno e possui diversos componentes, como plasma, leucócitos, hemácias e plaquetas.
Marcheze, Mariana Gonçalves, Freitas, Pablo Madson Oliveira, Ventura, Lucas Junior, Moreira, Camilly Teles, Santos, Joyce Nascimento, Cassiano, Júlia Camilo   +5 more
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