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Self-efficacy Affects Blood Sugar Control Among Adolescents With Type I Diabetes Mellitus

Journal of the Formosan Medical Association, 2010-07, Vol.109 (7), p.503-510

2010

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Lymphoblastic Lymphoma Arising at the Insulin Injection Sites in a Child with Type 1 Diabetes Mellitus

The Journal of pediatrics, 2010-12, Vol.157 (6), p.1043-1043.e1

2010

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Early development in Williams syndrome

Pediatrics international, 2008-04, Vol.50 (2), p.221-224

2008

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Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature

European journal of pediatrics, 2009-08, Vol.168 (8), p.919-923

2009

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Bone age cluster assessment and feature clustering analysis based on phalangeal image rough segmentation

Pattern recognition, 2012, Vol.45 (1), p.322-332

2012

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Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

Journal of the American Society of Nephrology, 2005-10, Vol.16 (10), p.3061-3069

2005

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Seventeen Alpha-hydroxylase Deficiency

Journal of the Formosan Medical Association, 2006, Vol.105 (2), p.177-181

2006

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Height and Weight Growth in Children With Vesicoureteral Reflux Diagnosed Before One Year Old

Urology (Ridgewood, N.J.), 2009-12, Vol.74 (6), p.1314-1317

2009

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Bone mineral density and correlation factor analysis in normal Taiwanese children

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2007-11, Vol.48 (6), p.323

Shu, San-Ging

2007

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Anthropometric and Intellectual Evaluation of Individuals with Prader-Willi Syndrome

Journal of the Formosan Medical Association, 2007, Vol.106 (6), p.509-512

2007

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Maple syrup urine disease in the Austronesian aboriginal tribe Paiwan of Taiwan: a novel DBT (E2) gene 4.7 kb founder deletion caused by a nonhomologous recombination between LINE-1 and Alu and the carrier-frequency determination

European journal of human genetics : EJHG, 2003-12, Vol.11 (12), p.931-936

2003

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Alpha-gamma equalization-enhanced hand radiographic image segmentation scheme

Optical engineering, 2009-10, Vol.48 (10), p.107001

Shu, San-Ging

2009

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High resolution melting analysis for mutation detection for PTPN11 gene: Applications of this method for diagnosis of Noonan syndrome

Clinica chimica acta, 2009-11, Vol.409 (1), p.75-77

2009

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Corrigendum to “High resolution melting analysis for mutation detection for PTPN11 gene: Applications of this method for diagnosis of Noonan syndrome” [Clinica Chimica Acta 409 (1-2) (2009) 75-77]

Clinica chimica acta, 2010-02, Vol.411 (3), p.297-297

2010

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Pseudohypoparathyroidism: report of seven cases

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2005-11, Vol.46 (6), p.374

2005

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The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency

Molecular genetics and metabolism, 2009-05, Vol.97 (1), p.75-79

2009

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Successful Treatment of Acute Pancreatitis with Hydrocortisone in a Patient Postadrenalectomy

Digestive diseases and sciences, 2007-12, Vol.52 (12), p.3355-3357

2007

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Detection of Novel CFTR Mutations in Taiwanese Cystic Fibrosis Patients

Journal of the Formosan Medical Association, 2003-05, Vol.102 (5), p.287-291

2003

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A Mucolipidosis III Patient Presenting Characteristic Sonographic and Magnetic Resonance Imaging Findings of Claw Hand Deformity

Journal of the Formosan Medical Association, 2004-09, Vol.103 (9), p.715-720

2004

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Wolfram Syndrome: Phenotype and Novel Mutation in Two Taiwanese Siblings

Journal of the Formosan Medical Association, 2003-11, Vol.102 (11), p.808-811

2003

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Outcome of antithyroid medication and radioiodine therapy in pediatric Graves' disease

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2003-07, Vol.44 (4), p.220

2003

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Clinical evaluation of short children referred by school screening: an analysis of 655 children

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2002-11, Vol.43 (6), p.340

2002

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A child with primary germ cell tumor of the liver

Acta oncologica, 2007, Vol.46 (8), p.1198-1199

2007

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Unstratified Chemotherapy for Non-Metastatic Osteosarcoma of the Extremities in Children

Journal of the Formosan Medical Association, 2003-06, Vol.102 (6), p.387-393

2003

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Anthropometric and Intellectual Evaluation of Individuals with Prader-Willi Syndrome

Journal of the Formosan Medical Association, 2007-06, Vol.106 (6), p.509-512

2007

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Self-efficacy Affects Blood Sugar Control Among Adolescents With Type I Diabetes Mellitus

Lymphoblastic Lymphoma Arising at the Insulin Injection Sites in a Child with Type 1 Diabetes Mellitus

Early development in Williams syndrome

Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature

Bone age cluster assessment and feature clustering analysis based on phalangeal image rough segmentation

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

Seventeen Alpha-hydroxylase Deficiency

Height and Weight Growth in Children With Vesicoureteral Reflux Diagnosed Before One Year Old

Bone mineral density and correlation factor analysis in normal Taiwanese children

Anthropometric and Intellectual Evaluation of Individuals with Prader-Willi Syndrome

Maple syrup urine disease in the Austronesian aboriginal tribe Paiwan of Taiwan: a novel DBT (E2) gene 4.7 kb founder deletion caused by a nonhomologous recombination between LINE-1 and Alu and the carrier-frequency determination

Alpha-gamma equalization-enhanced hand radiographic image segmentation scheme

High resolution melting analysis for mutation detection for PTPN11 gene: Applications of this method for diagnosis of Noonan syndrome

Corrigendum to “High resolution melting analysis for mutation detection for PTPN11 gene: Applications of this method for diagnosis of Noonan syndrome” [Clinica Chimica Acta 409 (1-2) (2009) 75-77]

Pseudohypoparathyroidism: report of seven cases

The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency

Successful Treatment of Acute Pancreatitis with Hydrocortisone in a Patient Postadrenalectomy

Detection of Novel CFTR Mutations in Taiwanese Cystic Fibrosis Patients

A Mucolipidosis III Patient Presenting Characteristic Sonographic and Magnetic Resonance Imaging Findings of Claw Hand Deformity

Wolfram Syndrome: Phenotype and Novel Mutation in Two Taiwanese Siblings

Outcome of antithyroid medication and radioiodine therapy in pediatric Graves' disease

Clinical evaluation of short children referred by school screening: an analysis of 655 children

A child with primary germ cell tumor of the liver

Unstratified Chemotherapy for Non-Metastatic Osteosarcoma of the Extremities in Children

Anthropometric and Intellectual Evaluation of Individuals with Prader-Willi Syndrome

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