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Wei-De Lin

Showing results (71-80 of 93) with videos related to

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Stroke|November 30, 2021
Kawasaki Disease May Increase the Risk of Subsequent Cerebrovascular DiseaseChien-Heng Lin, Jung-Nien Lai, Inn-Chi Lee, et al.
In Vivo (Athens, Greece)|September 13, 2022
CD3<sup>+</sup>CD56<sup>+</sup> T Lymphocytes Are Associated With ER Stress and Inflammasome Activation in Type 1 DiabetesYu-Nan Huang, Wei-DE Lin, Pen-Hua Su, et al.
Biomedicine|December 19, 2014
Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutationI-Ching Chou, Sheng-Shing Lin, Wei-De Lin, et al.
American Journal of Medical Genetics. Part A|November 19, 2009
Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX maleShu-Chin Chien, Yueh-Chun Li, Ming Ho, et al.
Rapid Communications in Mass Spectrometry : RCM|May 19, 2007
Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometryWei-Yi Hsu, Wan-Yu Lo, Chien-Chen Lai, et al.
Human Mutation|February 2, 2017
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib AnomaliesChi-Fan Yang, Chung-Hsing Wang, Weng Siong H'ng, et al.
Anticancer Research|March 25, 2010
Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in TaiwanKang-Hsi Wu, Chung-Hsing Wang, Yung-Li Yang, et al.
Healthcare (Basel, Switzerland)|May 27, 2023
Acupuncture Decreases Risk of Hypertension in Patients with Chronic Spontaneous Urticaria in Taiwan: A Nationwide StudyHeng-Wei Chang, Wei-De Lin, Pai-Jun Shih, et al.
Clinical Chemistry and Laboratory Medicine|February 27, 2010
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndromeWei-De Lin, I-Ching Chou, Ni-Chung Lee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2008
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patientsWei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Stroke|November 30, 2021
Kawasaki Disease May Increase the Risk of Subsequent Cerebrovascular DiseaseChien-Heng Lin, Jung-Nien Lai, Inn-Chi Lee, et al.
In Vivo (Athens, Greece)|September 13, 2022
CD3<sup>+</sup>CD56<sup>+</sup> T Lymphocytes Are Associated With ER Stress and Inflammasome Activation in Type 1 DiabetesYu-Nan Huang, Wei-DE Lin, Pen-Hua Su, et al.
Biomedicine|December 19, 2014
Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutationI-Ching Chou, Sheng-Shing Lin, Wei-De Lin, et al.
American Journal of Medical Genetics. Part A|November 19, 2009
Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX maleShu-Chin Chien, Yueh-Chun Li, Ming Ho, et al.
Rapid Communications in Mass Spectrometry : RCM|May 19, 2007
Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometryWei-Yi Hsu, Wan-Yu Lo, Chien-Chen Lai, et al.
Human Mutation|February 2, 2017
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib AnomaliesChi-Fan Yang, Chung-Hsing Wang, Weng Siong H'ng, et al.
Anticancer Research|March 25, 2010
Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in TaiwanKang-Hsi Wu, Chung-Hsing Wang, Yung-Li Yang, et al.
Healthcare (Basel, Switzerland)|May 27, 2023
Acupuncture Decreases Risk of Hypertension in Patients with Chronic Spontaneous Urticaria in Taiwan: A Nationwide StudyHeng-Wei Chang, Wei-De Lin, Pai-Jun Shih, et al.
Clinical Chemistry and Laboratory Medicine|February 27, 2010
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndromeWei-De Lin, I-Ching Chou, Ni-Chung Lee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2008
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patientsWei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, et al.
Pageof 10