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Improved treatment results for childhood acute myeloid leukemia in Taiwan

Leukemia, 2006-01, Vol.20 (1), p.136-141

2006

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Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutations

Journal of endocrinology, 2002-03, Vol.172 (3), p.627-635

2002

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Modeling of a flexible beam actuated by shape memory alloy wires

Smart materials and structures, 1997-06, Vol.6 (3), p.265-277

1997

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A novel mutation in neonatal isolated sulphite oxidase deficiency

Neuropediatrics, 2002-08, Vol.33 (4), p.174-179

2002

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Mutations of CTNS Causing Intermediate Cystinosis

Molecular genetics and metabolism, 1999-08, Vol.67 (4), p.283-293

1999

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Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese

Human genetics, 1998-09, Vol.103 (3), p.304-310

1998

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The promoter region of the CTLA4 gene is associated with type 1 diabetes mellitus

Journal of Pediatric Endocrinology and Metabolism, 2001-04, Vol.14 (4), p.383

2001

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Residual deformation of active structures with SMA actuators

International journal of mechanical sciences, 1999-06, Vol.41 (6), p.595-619

1999

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Aldosterone-secreting adrenal cortical adenoma in a 11-year-old child and collective review of the literature

European journal of pediatrics, 1994-07, Vol.153 (7), p.480-482

1994

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Genetic analysis of the glucose-6-phosphatase mutation of type 1a glycogen storage disease in a Chinese family

Clinical genetics, 1996-10, Vol.50 (4), p.206-211

1996

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An 11-year old boy with short stature, psychomotor retardation and seizure

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2001-11, Vol.42 (6), p.325

Shu, S G

2001

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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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Transient neonatal hypoparathyroidism: report of four cases

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2001-11, Vol.42 (6), p.359

2001

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Novel cystic fibrosis mutation (2215insG) in two adolescent Taiwanese siblings

Journal of the Formosan Medical Association, 2000-07, Vol.99 (7), p.564-567

2000

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Growth response and final height in growth hormone-deficient patients treated with biosynthetic growth hormone

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2001-09, Vol.42 (5), p.291

2001

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Precocious puberty associated with growth hormone deficiency in a patient with craniopharyngioma: report of one case

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi, 2001-07, Vol.42 (4), p.243

2001

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Primary intracranial germ-cell tumor in children

Zhonghua yi xue za zhi (Taipei, Taiwan), 1997-11, Vol.60 (5), p.259

1997

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Aldosterone-secreting adrenal cortical adenoma in a 11-year-old child and collective review of the literature

European journal of pediatrics, 1994-10, Vol.153 (10), p.715-717

1994

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The efficacy of intranasal DDAVP therapy in children with nocturnal enuresis

Zhonghua yi xue za zhi (Taipei, Taiwan), 1993-12, Vol.52 (6), p.368

1993

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Langerhans cell histiocytosis: a 10-year review

Zhonghua minguo xiaoerke yixuehui zazhi, 1994-09, Vol.35 (5), p.385

1994

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Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan

Journal of the Formosan Medical Association, 1998-03, Vol.97 (3), p.186-190

1998

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Hyperglycemia induced by chemotherapeutic agents used in acute lymphoblastic leukemia: report of three cases

Zhonghua yi xue za zhi (Taipei, Taiwan), 1993-06, Vol.51 (6), p.457

1993

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Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of an X-Y homologous region

Zhonghua minguo xiaoerke yixuehui zazhi, 1996-05, Vol.37 (3), p.185

1996

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Cranial computed tomography in children with acute lymphoblastic leukemia after prophylactic treatment with cranial radiation therapy and intrathecal methotrexate

Cancer, 1993-03, Vol.71 (6), p.2105-2108

1993

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Factor VII deficiency with intracranial hemorrhage: a case report

Zhonghua yi xue za zhi (Taipei, Taiwan), 1993-09, Vol.52 (3), p.190

1993

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Improved treatment results for childhood acute myeloid leukemia in Taiwan

Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutations

Modeling of a flexible beam actuated by shape memory alloy wires

A novel mutation in neonatal isolated sulphite oxidase deficiency

Mutations of CTNS Causing Intermediate Cystinosis

Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese

The promoter region of the CTLA4 gene is associated with type 1 diabetes mellitus

Residual deformation of active structures with SMA actuators

Aldosterone-secreting adrenal cortical adenoma in a 11-year-old child and collective review of the literature

Genetic analysis of the glucose-6-phosphatase mutation of type 1a glycogen storage disease in a Chinese family

An 11-year old boy with short stature, psychomotor retardation and seizure

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

Transient neonatal hypoparathyroidism: report of four cases

Novel cystic fibrosis mutation (2215insG) in two adolescent Taiwanese siblings

Growth response and final height in growth hormone-deficient patients treated with biosynthetic growth hormone

Precocious puberty associated with growth hormone deficiency in a patient with craniopharyngioma: report of one case

Primary intracranial germ-cell tumor in children

Aldosterone-secreting adrenal cortical adenoma in a 11-year-old child and collective review of the literature

The efficacy of intranasal DDAVP therapy in children with nocturnal enuresis

Langerhans cell histiocytosis: a 10-year review

Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan

Hyperglycemia induced by chemotherapeutic agents used in acute lymphoblastic leukemia: report of three cases

Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of an X-Y homologous region

Cranial computed tomography in children with acute lymphoblastic leukemia after prophylactic treatment with cranial radiation therapy and intrathecal methotrexate

Factor VII deficiency with intracranial hemorrhage: a case report

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