Marfan Syndrome, Hypertrophic Cardiomyopathy And Long QT A Rare Association Causing Sudden Death. [PDF]
Carvalho D +6 more
europepmc +1 more source
Clinical, Laboratory, and Imaging Profile in Patients with Systemic Amyloidosis in a Brazilian Cardiology Referral Center. [PDF]
Fernandes F +20 more
europepmc +1 more source
Isolated renal glucosuria due to SLC5A2 gene mutation: a rare presentation. [PDF]
Dua P, Singh A, Mishra OP.
europepmc +1 more source
Compound Heterozygous Familial Hypercholesterolemia Caused by LDLR Variants. [PDF]
Pamplona-Cunha H +4 more
europepmc +1 more source
FLNC Associated Restrictive Cardiomyopathy and Hypertrabeculation, a Rare Association. [PDF]
Aristizabal AM +6 more
europepmc +1 more source
Renal tubular acidosis in hereditary transthyretin amyloidosis (ATTRv). [PDF]
Fernandes PC +3 more
europepmc +1 more source
A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report. [PDF]
Carvalho AA +6 more
europepmc +1 more source
One Patient, Two Cardiomyopathies. [PDF]
Strong C +4 more
europepmc +1 more source
Detecting Familial Hypercholesterolemia in Adolescents: Universal Screening is Key. [PDF]
Cesena FY.
europepmc +1 more source

