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Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report

World journal of clinical cases, 2022, Vol.10 (2), p.703-708

2022

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The management of a duodenal fistula involving the right hepatic duct: a rare case report

Frontiers in medicine, 2024, Vol.11, p.1346590-1346590

2024

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Omadacycline for the Treatment of Severe Chlamydia psittaci Pneumonia Complicated with Guillain-Barre Syndrome

Infection and drug resistance, 2024, Vol.17, p.81-87

2024

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Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)

Hemoglobin, 2022, Vol.46 (4), p.253-255

2022

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Duodenal obstruction associated with a ruptured pancreaticoduodenal artery aneurysm

Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva, 2022, Vol.114 (7), p.438-439

2022

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Acquired Digital Fibrokeratoma: A Report of Five Cases and Review of the Literature

Clinical, cosmetic and investigational dermatology, 2024, Vol.17, p.247-252

2024

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Thoracoscopic and endoscopic cooperative surgery for a giant esophageal leiomyoma

Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society, 2019, Vol.31 (5), p.590-590

2019

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Case report: A novel variant (H49N) in Myelin Protein Zero gene is responsible for a patient with Charcot-Marie-Tooth disease

Frontiers in neurology, 2024, Vol.15, p.1319962-1319962

2024

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Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus

Frontiers in genetics, 2023, Vol.14, p.1208540-1208540

2023

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Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient

Frontiers in genetics, 2023, Vol.14, p.1205052-1205052

2023

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CD4+ T cell count in HIV/TB co-infection and co-occurrence with HL: Case report and literature review

Open life sciences, 2023, Vol.18 (1), p.20220744-20220744

2023

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The Clinical Efficacy of Microsuture Technique Combined With Voice Therapy in Patients with Reinke's Edema

Journal of voice : official journal of the Voice Foundation, 2022

2022

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Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.132C>G) in a Chinese Family

Hemoglobin, 2022, Vol.46 (6), p.347-350

2022

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Wandering small intestinal stromal tumor: A case report

World journal of clinical cases, 2022, Vol.10 (29), p.10622-10628

2022

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Osteogenesis imperfecta type VIII: Association with increased nuchal translucency and prenatal diagnosis by targeted exome sequencing

European journal of obstetrics, gynecology, and reproductive biology, 2019, Vol.235, p.128-129

2019

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Acute carotid stent thrombosis: A case report and literature review

World journal of clinical cases, 2022, Vol.10 (26), p.9310-9317

2022

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A case report of Erdheim-Chester disease-clinically characterized by recurrent fever, multiple bone destruction, and antinuclear antibodies

Heliyon, 2023, Vol.9 (8), p.e18867-e18867

2023

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Design strategy of TiC reinforced heterogeneous Ti-composites with an induced <c + a> slip system for achieving high strength-ductility

Materials Research Letters, 2024, Vol.12 (4), p.298-305

2024

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Pediatric Giant Craniopharyngioma: Surgical Field Soak in Diluted Nimodipine Solution Reduces Cerebral Vasospasm

World neurosurgery, 2020, Vol.141, p.113-113

2020

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β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report

Hemoglobin, 2022, Vol.46 (2), p.137-139

2022

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Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)

Hemoglobin, 2022, Vol.46 (2), p.129-131

2022

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Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)

Frontiers in genetics, 2022, Vol.13, p.887082-887082

2022

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Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing

Cytogenetic and genome research, 2022, Vol.162 (7), p.386-390

2022

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Tigliane-and daphnane-type diterpenoids from the buds of Daphne genkwa with their cytotoxic activities

Natural Product Research, 2023, Vol.37 (18), p.3163-3169

2023

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Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report

Hemoglobin, 2021, Vol.45 (5), p.329-331

2021

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Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report

The management of a duodenal fistula involving the right hepatic duct: a rare case report

Omadacycline for the Treatment of Severe Chlamydia psittaci Pneumonia Complicated with Guillain-Barre Syndrome

Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)

Duodenal obstruction associated with a ruptured pancreaticoduodenal artery aneurysm

Acquired Digital Fibrokeratoma: A Report of Five Cases and Review of the Literature

Thoracoscopic and endoscopic cooperative surgery for a giant esophageal leiomyoma

Case report: A novel variant (H49N) in Myelin Protein Zero gene is responsible for a patient with Charcot-Marie-Tooth disease

Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus

Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient

CD4+ T cell count in HIV/TB co-infection and co-occurrence with HL: Case report and literature review

The Clinical Efficacy of Microsuture Technique Combined With Voice Therapy in Patients with Reinke's Edema

Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.132C>G) in a Chinese Family

Wandering small intestinal stromal tumor: A case report

Osteogenesis imperfecta type VIII: Association with increased nuchal translucency and prenatal diagnosis by targeted exome sequencing

Acute carotid stent thrombosis: A case report and literature review

A case report of Erdheim-Chester disease-clinically characterized by recurrent fever, multiple bone destruction, and antinuclear antibodies

Design strategy of TiC reinforced heterogeneous Ti-composites with an induced <c + a> slip system for achieving high strength-ductility

Pediatric Giant Craniopharyngioma: Surgical Field Soak in Diluted Nimodipine Solution Reduces Cerebral Vasospasm

β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report

Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)

Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)

Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing

Tigliane-and daphnane-type diterpenoids from the buds of Daphne genkwa with their cytotoxic activities

Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report

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