Sage Journals: Discover world-class research

Open access

Case report

First published 2024

Heterozygous MEFV Mutation Leading to Renal Failure: A Case Study

Souhaila El Gazzane, Amine Ichane, Chaimae Nahi [...]

Sage Open Pediatrics

Retricted access

Case report

First published 2014-9

Recurrent Venous Thromboembolism in a Patient with Heterozygous Factor V Leiden Mutation

C. Whitney White, Angela R. Thomason, Valerie Prince

Hospital Pharmacy

Open access

Case report

First published 2019-9

Complex medical history of a patient with a compound heterozygous mutation in C1QC

R Lubbers, L J J Beaart-van de Voorde, K van Leeuwen [...]

Lupus

Retricted access

Research article

First published 2026-4

Clinical and Biological Phenotypes of Patients Carrying a Heterozygous Variant in Genes of Leptin-Melanocortin Signaling Pathway

Elsa Dieterlen, Delphine Collin-Chavagnac, Bérénice Segrestin [...]

Childhood Obesity

Open access

Article commentary

First published 2018

CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?

Giorgia Canali, Laurence Goutebroze

Neuroscience Insights

Retricted access

Research article

First published 1988-8

Blood rheology and red cell metabolism in the menstrual cycle in normal and heterozygous thalassemic women

A.A. Kaperonis, S. Chien

Clinical Hemorheology and Microcirculation

Retricted access

Research article

First published 2004-10

The relationship between the enzyme activity,lipid peroxidation and red blood cells deformability in hemizygous and heterozygous glucose‐6‐phosphate dehydrogenase deficient individuals

N. Gurbuz, O. Yalcin, T.A. Aksu [...]

Clinical Hemorheology and Microcirculation

Retricted access

Research article

First published 2004-10

The relationship between the enzyme activity,lipid peroxidation and red blood cells deformability in hemizygous and heterozygous glucose‐6‐phosphate dehydrogenase deficient individuals

N. Gurbuz, O. Yalcin, T.A. Aksu [...]

Clinical Hemorheology and Microcirculation

Retricted access

Case report

First published 2017-12

The first Greek case of heterozygous cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy: An atypical clinico-radiological presentation

Anastasia Bougea, George Velonakis, Nikolaos Spantideas [...]

The Neuroradiology Journal

Open access

Case report

First published 2021-4

Heterozygous desmin gene ( DES ) mutation contributes to familial dilated cardiomyopathy

Ying-shuo Huang, Yun-li Xing, Hong-wei Li

Journal of International Medical Research

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