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Psychosomatic and physical responses to a multi-component stress management program among teaching professionals: A randomized study of cognitive behavioral intervention (CB) with complementary and alternative medicine (CAM) approach

Behaviour research and therapy, 2016-05, Vol.80, p.10-16

2016

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Intra-Renal and Subcellular Distribution of the Human Chloride Channel, CLC-5, Reveals a Pathophysiological Basis for Dent's Disease

Human molecular genetics, 1999-02, Vol.8 (2), p.247-257

1999

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Recruitment of African American Men: Overcoming Challenges for an Epidemiological Study of Personality and Health

Cultural diversity & ethnic minority psychology, 2011-10, Vol.17 (4), p.377-380

2011

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Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene

Nature clinical practice. Endocrinology & metabolism, 2008-01, Vol.4 (1), p.53-58

2008

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Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1

American journal of human genetics, 1998-02, Vol.62 (2), p.232-244

1998

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OCRL1 Mutations in Dent 2 Patients Suggest a Mechanism for Phenotypic Variability

Nephron. Physiology, 2009-01, Vol.112 (2), p.p27-p36

2009

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Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

The journal of clinical endocrinology and metabolism, 2012-10, Vol.97 (10), p.E1995-E2005

2012

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MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)

The Journal of clinical investigation, 2005-10, Vol.115 (10), p.2832-2842

2005

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Depression and anxiety among university students in Hong Kong

Hong Kong medical journal = Xianggang yi xue za zhi, 2018-10, Vol.24 (5), p.466

2018

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X-Linked Hypophosphatemia Attributable to Pseudoexons of the PHEX Gene

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3840-3844

2001

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Mutational analysis of PHEX gene in X-linked hypophosphatemia

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3615-3623

1998

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Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis

Journal of bone and mineral research, 2019-07, Vol.34 (7), p.1324-1335

2019

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Pseudohypoparathyroidism type 1a due to a novel mutation in the GNAS gene

Clinical endocrinology (Oxford), 2016-03, Vol.84 (3), p.463-465

2016

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A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia

Clinical endocrinology (Oxford), 2010-12, Vol.73 (6), p.715-722

2010

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Asymptomatic Children with Multiple Endocrine Neoplasia Type 1 Mutations May Harbor Nonfunctioning Pancreatic Neuroendocrine Tumors

The journal of clinical endocrinology and metabolism, 2009-10, Vol.94 (10), p.3640-3646

2009

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Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1)

Human mutation, 2010, Vol.31 (1), p.E1089-E1101

2010

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Characteristics of Hearing Loss in HDR (Hypoparathyroidism, Sensorineural Deafness, Renal Dysplasia) Syndrome

Audiology & neurotology, 2006-01, Vol.11 (6), p.373-379

2006

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Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3233-3236

2001

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A Novel EXT1 Splice Site Mutation in a Kindred with Hereditary Multiple Exostosis and Osteoporosis

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5386-5392

2005

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Adult‐Onset Facial Colloid Milium Successfully Treated with the Long‐Pulsed Er:YAG Laser

Dermatologic surgery, 2002-03, Vol.28 (3), p.215-219

2002

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Renal Chloride Channel, CLCN5, Mutations in Dent's Disease

Journal of bone and mineral research, 1999-09, Vol.14 (9), p.1536-1542

1999

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Detection of KRAS mutations in liquid biopsies from metastatic colorectal cancer patients using droplet digital PCR, Idylla, and next generation sequencing

PloS one, 2020-11, Vol.15 (11), p.e0239819

2020

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A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3343-3347

2000

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Long-term upregulation of inflammation and suppression of cell proliferation in the brain of adult rats exposed to traumatic brain injury using the controlled cortical impact model

PloS one, 2013-01, Vol.8 (1), p.e53376-e53376

2013

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Psychosomatic and physical responses to a multi-component stress management program among teaching professionals: A randomized study of cognitive behavioral intervention (CB) with complementary and alternative medicine (CAM) approach

Intra-Renal and Subcellular Distribution of the Human Chloride Channel, CLC-5, Reveals a Pathophysiological Basis for Dent's Disease

Recruitment of African American Men: Overcoming Challenges for an Epidemiological Study of Personality and Health

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene

Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1

OCRL1 Mutations in Dent 2 Patients Suggest a Mechanism for Phenotypic Variability

Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)

Depression and anxiety among university students in Hong Kong

X-Linked Hypophosphatemia Attributable to Pseudoexons of the PHEX Gene

Mutational analysis of PHEX gene in X-linked hypophosphatemia

Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis

Pseudohypoparathyroidism type 1a due to a novel mutation in the GNAS gene

A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia

Asymptomatic Children with Multiple Endocrine Neoplasia Type 1 Mutations May Harbor Nonfunctioning Pancreatic Neuroendocrine Tumors

Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1)

Characteristics of Hearing Loss in HDR (Hypoparathyroidism, Sensorineural Deafness, Renal Dysplasia) Syndrome

Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda

A Novel EXT1 Splice Site Mutation in a Kindred with Hereditary Multiple Exostosis and Osteoporosis

Adult‐Onset Facial Colloid Milium Successfully Treated with the Long‐Pulsed Er:YAG Laser

Renal Chloride Channel, CLCN5, Mutations in Dent's Disease

Detection of KRAS mutations in liquid biopsies from metastatic colorectal cancer patients using droplet digital PCR, Idylla, and next generation sequencing

A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred

Long-term upregulation of inflammation and suppression of cell proliferation in the brain of adult rats exposed to traumatic brain injury using the controlled cortical impact model

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