Gene Symbol: VMD2. Disease: Best vitelliform macular dystrophy (VMD2)

[Clinical characteristics of regional portal hypertension in children presenting with isolated gastric fundal varices].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2026

[Current status and temporal trends in osteoarthritis burden in China: an age-period-cohort analysis with projection].

Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi·2026

Combination of Measurements of CP Properties of Higgs Boson Interactions with Vector Bosons Using Proton-Proton Collisions at sqrt[s]=13 TeV with the ATLAS Detector.

Physical review letters·2026

[Research progress in artificial intelligence-driven digital removable partial denture clinical diagnosis and treatment].

Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology·2026

[The effect of the PI3K/Akt/HIF-1α signaling pathway in the changes of urinary metabolite in silicosis mice model].

Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases·2026

[A dual-center study of enhanced CT-based nomograms predicts spontaneous portosystemic shunts on initial hemorrhage from rupture of esophageal gastric varices in cirrhosis].

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology·2026

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

Human genetics·2026

CRISPR/Cas9-based repair of a heterozygous HNF1A mutation in patient-derived hiPSCs.

Human genetics·2026

TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processing.

Human genetics·2026

The Russian FSHD registry: a first look at the cohort.

Human genetics·2026

Genetic ancestry of the Mulam ethnic group: admixture from ancient Yellow River, southern native, and Austronesian populations.

Human genetics·2026

Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension.

Human genetics·2026

Comparative Evaluation of MRI and Ultrasonography for Temporomandibular Joint Pathologies with Emphasis on Bone Marrow Edema.

Dento maxillo facial radiology·2026

Arrhythmogenic Mitral Valve Prolapse: Looking Beyond Mitral Regurgitation.

JACC. Case reports·2026

Challenges in the management of Melkersson-Rosenthal syndrome: a case report and systematic review.

General dentistry·2026

Innocent Until Proven Guilty: Native Valve Staphylococcus lugdunensis Infective Endocarditis Complicated by Embolic Stroke in a Peritoneal Dialysis Patient: A Case Report.

Journal of community hospital internal medicine perspectives·2026

Deep-Seated Kaposiform Hemangioendothelioma Presenting with Recurrent Hemorrhagic Episodes: A Diagnostic Challenge.

Case reports in oncology·2026

Clade-specific multiplex digital PCR assay for monkeypox virus detection in spike-in wastewater samples.

Access microbiology·2026

Related Experiment Videos

Gene Symbol: VMD2. Disease: Best vitelliform macular dystrophy (VMD2)

Related Concept Videos

[Clinical characteristics of regional portal hypertension in children presenting with isolated gastric fundal varices].

[Current status and temporal trends in osteoarthritis burden in China: an age-period-cohort analysis with projection].

Combination of Measurements of CP Properties of Higgs Boson Interactions with Vector Bosons Using Proton-Proton Collisions at sqrt[s]=13 TeV with the ATLAS Detector.

[Research progress in artificial intelligence-driven digital removable partial denture clinical diagnosis and treatment].

[The effect of the PI3K/Akt/HIF-1α signaling pathway in the changes of urinary metabolite in silicosis mice model].

[A dual-center study of enhanced CT-based nomograms predicts spontaneous portosystemic shunts on initial hemorrhage from rupture of esophageal gastric varices in cirrhosis].

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

CRISPR/Cas9-based repair of a heterozygous HNF1A mutation in patient-derived hiPSCs.

TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processing.

The Russian FSHD registry: a first look at the cohort.

Genetic ancestry of the Mulam ethnic group: admixture from ancient Yellow River, southern native, and Austronesian populations.

Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension.

Comparative Evaluation of MRI and Ultrasonography for Temporomandibular Joint Pathologies with Emphasis on Bone Marrow Edema.

Arrhythmogenic Mitral Valve Prolapse: Looking Beyond Mitral Regurgitation.

Challenges in the management of Melkersson-Rosenthal syndrome: a case report and systematic review.

Innocent Until Proven Guilty: Native Valve Staphylococcus lugdunensis Infective Endocarditis Complicated by Embolic Stroke in a Peritoneal Dialysis Patient: A Case Report.

Deep-Seated Kaposiform Hemangioendothelioma Presenting with Recurrent Hemorrhagic Episodes: A Diagnostic Challenge.

Clade-specific multiplex digital PCR assay for monkeypox virus detection in spike-in wastewater samples.

Related Experiment Videos

Gene Symbol: VMD2. Disease: Best vitelliform macular dystrophy (VMD2)

Related Concept Videos

Related Articles