Results 121 to 130 of about 97,051 (153)

Marfan Syndrome, Hypertrophic Cardiomyopathy And Long QT A Rare Association Causing Sudden Death. [PDF]

Arq Bras Cardiol
Carvalho D, Carvalho S, Pacheco A, Costa C, Carvalho P, Ferreira R, Briosa A.   +6 more
europepmc   +1 more source

Clinical, Laboratory, and Imaging Profile in Patients with Systemic Amyloidosis in a Brazilian Cardiology Referral Center. [PDF]

Arq Bras Cardiol, 2022
Fernandes F, Alencar Neto AC, Bueno BVK, Cafezeiro CRF, Rissato JH, Szor RS, Carvalho MLP, Mathias Júnior W, Lino AMM, Castelli JB, Souza EO, Ramires FJA, Hotta VT, Soares Júnior J, Tavares CAM, Krieger JE, Rochitte CE, Dabarian A, Hajjar LA, Kalil Filho R, Mady C.   +20 more
europepmc   +1 more source

Isolated renal glucosuria due to SLC5A2 gene mutation: a rare presentation. [PDF]

J Bras Nefrol
Dua P, Singh A, Mishra OP.
europepmc   +1 more source

Diagnosis of MALT Lymphoma from Surveillance Endoscopy of a Patient with a CDH1 Gene Germline Mutation. [PDF]

GE Port J Gastroenterol, 2022
Pinto C, Cunha AL, Rodrigues Â, Dias R, Brandão C, Dinis-Ribeiro M.   +5 more
europepmc   +1 more source

Trombose Venosa Esplâncnica: Factores de Risco [PDF]

, 2012
Tiago Alexandre Espada Guerreiro
core  

FLNC Associated Restrictive Cardiomyopathy and Hypertrabeculation, a Rare Association. [PDF]

Arq Bras Cardiol
Aristizabal AM, Guzmán-Serrano CA, Lizcano MI, Mosquera W, Lores J, Pachajoa H, Cely C.   +6 more
europepmc   +1 more source

Compound Heterozygous Familial Hypercholesterolemia Caused by LDLR Variants. [PDF]

Arq Bras Cardiol, 2020
Pamplona-Cunha H, Medeiros MF, Sincero TCM, Back IC, Silva ELD.   +4 more
europepmc   +1 more source

Detecting Familial Hypercholesterolemia in Adolescents: Universal Screening is Key. [PDF]

Arq Bras Cardiol
Cesena FY.
europepmc   +1 more source

Renal tubular acidosis in hereditary transthyretin amyloidosis (ATTRv). [PDF]

J Bras Nefrol
Fernandes PC, Silva MDD, Waddington-Cruz M, Gomes CP.   +3 more
europepmc   +1 more source

A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report. [PDF]

Rev Paul Pediatr
Carvalho AA, Machado RA, Maia CMF, Santos LAND, Martelli DRB, Coletta RD, Martelli Júnior H.   +6 more
europepmc   +1 more source