Namhee Kim

Assistant Professor

Dong-A University College of Medicine

South Korea

Research Interests

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Articles (13)

Year:

2024

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Collaborators (10)

Jae Min Lee

Associate Professor

Yeungnam University

SOUTH KOREA

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In Hwa Jeong

Dong-A University

SOUTH KOREA

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Sang Mee Hwang

Seoul National University Hospital

SOUTH KOREA

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Jieun Kim

Assistant Professor

Soonchunhyang University Hospital Bucheon

SOUTH KOREA

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Hyunyong Hwang

Kosin University Gospel Hospital

SOUTH KOREA

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Myungshin Kim

Professor

Catholic University of Korea School of Medicine

SOUTH KOREA

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Ye Jee Shim

Associate Professor

Keimyung University School of Medicine

SOUTH KOREA

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Hee won Chueh

Assistent Professor

Dong-A University Medical Center

SOUTH KOREA

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HYE LIM JUNG

Professor

Sungkyunkwan University School of Medicine

SOUTH KOREA

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Hyoung Soo Choi

SOUTH KOREA

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Namhee Kim

Research Interests

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Articles (13)

Current Status of Molecular Diagnosis of Hereditary Hemolytic Anemia in Korea

Congenital Factor V Deficiency from Compound Heterozygous Mutations with a Novel Variant c.5403del (p.Lys1801AsnfsTer11) in the F5 Gene: A Case Report

Missense Variant c.3301C>T (p.R1101W) in von Willebrand Factor A Sequence in a Patient with Recessive Dystrophic Epidermolysis Bullosa Pruriginosa with Compound Heterozygous COL7A1 Variants

Korean clinical practice guidelines for the diagnosis of hereditary hemolytic anemia.

Molecular genetic testing enabled the diagnosis of otherwise undiagnosable cases of pyruvate kinase deficiency

Evaluation of automated calibration and quality control processes using the Aptio total laboratory automation system

A Novel Germline Mutation in DDX41 Predisposed to Myelodysplasia/Acute Myeloid Leukemia

Guidelines for Genetic Counseling and Reporting of Cancer Genetic Test Results: Genetic Test for Hereditary Cancer-predisposing Syndrome Using Next-generation Sequencing

A novel variant of PHEX in a Korean family with X-linked hypophosphatemic rickets

Current Issues, Challenges, and Future Perspectives of Genetic Counseling in Korea

A pathogenic PHEX variant (c.1483-1G>C) in a Korean patient with X-linked hypophosphatemic rickets

Novel PKD1 Mutations in Patients with Autosomal Dominant Polycystic Kidney Disease

A Novel KCNA1 Mutation in an Episodic Ataxia Type 1 Patient with Asterixis and Falls

Collaborators (10)

Jae Min Lee

In Hwa Jeong

Sang Mee Hwang

Jieun Kim

Hyunyong Hwang

Myungshin Kim

Ye Jee Shim

Hee won Chueh

HYE LIM JUNG

Hyoung Soo Choi

Make your next move.

Namhee Kim

Research Interests

Explore related searches

Articles (13)

Current Status of Molecular Diagnosis of Hereditary Hemolytic Anemia in Korea

Congenital Factor V Deficiency from Compound Heterozygous Mutations with a Novel Variant c.5403del (p.Lys1801AsnfsTer11) in the F5 Gene: A Case Report

Missense Variant c.3301C>T (p.R1101W) in von Willebrand Factor A Sequence in a Patient with Recessive Dystrophic Epidermolysis Bullosa Pruriginosa with Compound Heterozygous COL7A1 Variants

Korean clinical practice guidelines for the diagnosis of hereditary hemolytic anemia.

Molecular genetic testing enabled the diagnosis of otherwise undiagnosable cases of pyruvate kinase deficiency

Evaluation of automated calibration and quality control processes using the Aptio total laboratory automation system

A Novel Germline Mutation in DDX41 Predisposed to Myelodysplasia/Acute Myeloid Leukemia

Guidelines for Genetic Counseling and Reporting of Cancer Genetic Test Results: Genetic Test for Hereditary Cancer-predisposing Syndrome Using Next-generation Sequencing

A novel variant of PHEX in a Korean family with X-linked hypophosphatemic rickets

Current Issues, Challenges, and Future Perspectives of Genetic Counseling in Korea

A pathogenic PHEX variant (c.1483-1G&gt;C) in a Korean patient with X-linked hypophosphatemic rickets

Novel PKD1 Mutations in Patients with Autosomal Dominant Polycystic Kidney Disease

A Novel KCNA1 Mutation in an Episodic Ataxia Type 1 Patient with Asterixis and Falls

Collaborators (10)

Jae Min Lee

In Hwa Jeong

Sang Mee Hwang

Jieun Kim

Hyunyong Hwang

Myungshin Kim

Ye Jee Shim

Hee won Chueh

HYE LIM JUNG

Hyoung Soo Choi

Make your next move.

A pathogenic PHEX variant (c.1483-1G>C) in a Korean patient with X-linked hypophosphatemic rickets