Sage Journals: Discover world-class research

Retricted access

Case report

First published 2001-12

Tuberous Sclerosis Complex with an Unruptured Intracranial Aneurysm: Manifestations of Contiguous Gene Syndrome

Y.L. Chen, C.B. Luo, S.W. Hsu [...]

Interventional Neuroradiology

Retricted access

Research article

First published 2024-3

TSC2/PKD1 Contiguous Gene Deletion Syndrome

Javier Arredondo Montero, Mónica Bronte Anaut, María Velayos [...]

Clinical Pediatrics

Retricted access

Other

First published 2008-10

Tuberous Sclerosis Complex With Polycystic Kidney Disease of the Adult Type: the TSC2/ADPKD1 Contiguous Gene Syndrome

Michele Bisceglia, Carlos Galliani, Illuminato Carosi [...]

International Journal of Surgical Pathology

Retricted access

Other

First published 2008-01

Persistent Growth Failure in Prader-Willi Syndrome Associated With Short-Chain Acyl-CoA Dehydrogenase Gene Variant

Dan-Victor Giurgiutiu, Lesby M. Espinoza, Tim C. Wood [...]

Journal of Child Neurology

Retricted access

Review article

First published 2001-06

Approaches to Gene Therapy for Human Immunodeficiency Virus Infection

Gary L. Buchschacher, Flossie Wong-Staal

Human Gene Therapy

Open access

Case report

First published 2021

Search for Genetic Predictors of Adult Autoimmune Polyendocrine Syndrome in Monozygotic Twins

Marina Yuryevna Yukina, Anna Aleksandrovna Larina, Evgeny Vitalyevich Vasilyev [...]

Clinical Medicine Insights: Endocrinology and Diabetes

Open access

Case report

First published 2014

A novel mutation in the succinate dehydrogenase subunit D gene in siblings with the hereditary paraganglioma–pheochromocytoma syndrome

Chaithra Prasad, Gerard J Oakley, Linwah Yip [...]

Sage Open Medical Case Reports

Open access

Review article

First published 2014

Current View of miRNA with Tumor Suppressor Function,Exploring MDS and AML as Models

Nicholas Iverson, Naomi Galili, Abdullah M. Ali [...]

Signal Transduction Insights

Retricted access

Research article

First published 2025-3

Comprehensive Clinical and Genetic Characterization of Kabuki Syndrome: A Case Series Study

Salvatore Michele Carnazzo, Desirèe Balconara, Francesco Caruso [...]

Journal of Child Neurology

Retricted access

Review article

First published 2012-06

Cell and Gene Therapy for Genetic Diseases: Inherited Disorders Affecting the Lung and Those Mimicking Sudden Infant Death Syndrome

Allison M. Keeler, Terence R. Flotte

Human Gene Therapy

Search results