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Academic Journal

Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population.

  • Authors : Li Y; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China.; Department Five of Neurology, Cangzhou Central Hospital, Yunhe District, Cangzhou, Hebei, China.

Subjects: Alzheimer Disease*/Alzheimer Disease*/Alzheimer Disease*/genetics ; Frontotemporal Lobar Degeneration*/Frontotemporal Lobar Degeneration*/Frontotemporal Lobar Degeneration*/genetics ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methods

  • Source: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2024; Vol. 99 (2), pp. 577-593.Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9814863 Publication Model: Print Cited Medium: Internet ISSN: 1875-8908

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Academic Journal

Epidemiological, clinical, pathological and genetic characteristics of epidermolysis bullosa in New Zealand.

Subjects: *EPIDERMOLYSIS bullosa; *ASIANS; *NURSING recordsNEW Zealand

  • Source: Australasian Journal of Dermatology. Feb2022, Vol. 63 Issue 1, p62-67. 6p. 4 Charts.

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Academic Journal

Cost-effectiveness of screening for HLA-B*1502 prior to initiation of carbamazepine in epilepsy patients of Asian ancestry in the United States.

  • Authors : Choi H; Department of Neurology, Columbia University, New York, New York.; Mohit B

Subjects: Anticonvulsants/Anticonvulsants/Anticonvulsants/*therapeutic use ; Asian People/Asian People/Asian People/*genetics ; Carbamazepine/Carbamazepine/Carbamazepine/*therapeutic use

  • Source: Epilepsia [Epilepsia] 2019 Jul; Vol. 60 (7), pp. 1472-1481. Date of Electronic Publication: 2019 Jun 03.Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Precision Therapy for a Chinese Family With Maturity-Onset Diabetes of the Young.

  • Authors : Li J; Department of Pharmacy, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.; Shu M

Subjects: Mutation* ; Precision Medicine*; Asian People/Asian People/Asian People/*genetics Maturity-Onset Diabetes of the Young, Type 2

  • Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2021 Aug 05; Vol. 12, pp. 700342. Date of Electronic Publication: 2021 Aug 05 (Print Publication: 2021).Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print

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Prenatal diagnosis of congenital nephrotic syndrome of the Finnish type in a Chinese family.

  • Authors : Gu Y; First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.; Han B

Subjects: Asian People/Asian People/Asian People/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Nephrotic Syndrome/Nephrotic Syndrome/Nephrotic Syndrome/*diagnosis Nephrosis, congenital

  • Source: Taiwanese journal of obstetrics & gynecology [Taiwan J Obstet Gynecol] 2021 Jul; Vol. 60 (4), pp. 758-762.Publisher: Elsevier Country of Publication: China (Republic : 1949- ) NLM ID: 101213819 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Genetic Analysis of ZNF Protein Family Members for Early-Onset Parkinson's Disease in Chinese Population.

  • Authors : Li CY; Department of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, No.37, Guoxue Lane, Chengdu, 610041, Sichuan, China.; Ou RW

Subjects: Asian People/Asian People/Asian People/*genetics ; DNA-Binding Proteins/DNA-Binding Proteins/DNA-Binding Proteins/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

  • Source: Molecular neurobiology [Mol Neurobiol] 2021 Jul; Vol. 58 (7), pp. 3435-3442. Date of Electronic Publication: 2021 Mar 15.Publisher: Humana Press Country of Publication: United States NLM ID: 8900963 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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A genetic test for three historical hypotheses of the Mongolian Golden family origin of Tusi Lu's family, a response to a commentary on molecular genealogy of Tusi Lu's family reveals their paternal relationship with Jochi, Genghis Khan's eldest son.

  • Authors : Wen SQ; MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, 200438, China.; Institute of Archaeological Science, Fudan University, Shanghai, 200433, China.

Subjects: Family* ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methods; Asian People/Asian People/Asian People/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2021 May; Vol. 66 (5), pp. 551-553. Date of Electronic Publication: 2020 Dec 05.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Race and Pharmacogenomics-Personalized Medicine or Misguided Practice?

  • Authors : Goodman CW; Department of Medicine, University of South Carolina School of Medicine, Columbia.; Brett AS

Subjects: Genetic Testing* ; Pharmacogenetics* ; Precision Medicine*

  • Source: JAMA [JAMA] 2021 Feb 16; Vol. 325 (7), pp. 625-626.Publisher: American Medical Association Country of Publication: United States NLM ID: 7501160 Publication Model: Print Cited Medium: Internet ISSN:

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