Results 61 to 70 of about 729 (115)

[Rh blood group: Review and importance of genotyping]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Campos-Aguirre E   +3 more
europepmc   +1 more source

Pericarditis severa como primera manifestación de una combinación de enfermedad autoinflamatoria genética y anemia genética. Reporte de caso

open access: yesRevista Paraguaya de Reumatología
La pericarditis es una de las enfermedades pericárdicas más frecuentes. La activación del inflamasoma NLRP3 (receptor de unión a nucleótidos y oligomerización (NOD) similar a (NLR) que contiene el dominio pirina (NLRP) 3) es central en la génesis de la ...
Irene Benítez   +4 more
doaj  

[Factors that interfere with the HbA1c result]. [PDF]

open access: yesAten Primaria
Ballesteros Merino M   +2 more
europepmc   +1 more source

Genetic atypical hemolytic uremic syndrome in children: a 20-year experience from a tertiary center. [PDF]

open access: yesJ Bras Nefrol, 2021
Maximiano C   +13 more
europepmc   +1 more source

[Cold agglutinin syndrome associated with infectious mononucleosis: A case report]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Garzón-Recalde DA   +2 more
europepmc   +1 more source

Microangiopatía trombótica (MAT) asociada al embarazo: papel del laboratorio clínico en el diagnóstico diferencial. [PDF]

open access: yesAdv Lab Med
Ramos Mayordomo P   +7 more
europepmc   +1 more source

Autoimmune hepatitis. Another consequence of COVID-19? [PDF]

open access: yesGastroenterol Hepatol, 2023
Andrés L   +7 more
europepmc   +1 more source

Thrombotic microangiopathy in patients with sickle cell disease. [PDF]

open access: yesRev Paul Pediatr
Carrasco GB, Blum PB, Braga JAP.
europepmc   +1 more source

Hemolytic disease of the fetus and newborn and Rhesus alloimmunization in Latin American countries: a scoping review. [PDF]

open access: yesBMC Pregnancy Childbirth
Júnior MDC   +5 more
europepmc   +1 more source

Recommendations for diagnosis and treatment of Atypical Hemolytic Uremic Syndrome (aHUS): an expert consensus statement from the Rare Diseases Committee of the Brazilian Society of Nephrology (COMDORA-SBN). [PDF]

open access: yesJ Bras Nefrol
Vaisbich MH   +15 more
europepmc   +1 more source

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