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Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma

Human genetics, 1998-10, Vol.103 (4), p.393-399

1998

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A two-hit model for developmental defects in Gorlin syndrome

Nature genetics, 1996-01, Vol.12 (1), p.85-87

1996

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Mutation Hotspots Due to Sunlight in the p53 Gene of Nonmelanoma Skin Cancers

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (9), p.4216-4220

1993

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Randomized Multicenter Clinical Trial of Myofascial Physical Therapy in Women With Interstitial Cystitis/Painful Bladder Syndrome and Pelvic Floor Tenderness

The Journal of urology, 2012-06, Vol.187 (6), p.2113-2118

2012

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Epidemiology of Congenital Cytomegalovirus Infection: Maternal Risk Factors and Molecular Analysis of Cytomegalovirus Strains

American journal of epidemiology, 1998-05, Vol.147 (10), p.940-947

1998

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Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial

The Lancet (British edition), 2010-01, Vol.375 (9712), p.385-395

2010

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MPPH Syndrome: Two New Cases

Pediatric neurology, 2011-05, Vol.44 (5), p.370-373

2011

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Effect of Amitriptyline on Symptoms in Treatment Naïve Patients With Interstitial Cystitis/Painful Bladder Syndrome

The Journal of urology, 2010-05, Vol.183 (5), p.1853-1858

2010

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Specialty care by child neurologists: a workforce analysis

Neurology, 2005-03, Vol.64 (6), p.942-948

2005

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Alfuzosin and Symptoms of Chronic Prostatitis–Chronic Pelvic Pain Syndrome

The New England journal of medicine, 2008-12, Vol.359 (25), p.2663-2673

2008

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Errors and error management in image-guided craniomaxillofacial surgery

Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 2009-05, Vol.107 (5), p.701-715

2009

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Relationship Between Sunlight Exposure and a Key Genetic Alteration in Basal Cell Carcinoma

JNCI : Journal of the National Cancer Institute, 1996-03, Vol.88 (6), p.349-354

1996

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Vitamin D receptor gene polymorphisms, serum 25-hydroxyvitamin D levels, and melanoma: UK case–control comparisons and a meta-analysis of published VDR data

European journal of cancer (1990), 2009-12, Vol.45 (18), p.3271-3281

2009

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The Spectrum of Pathogenic Mutations in SPINK5 in 19 Families with Netherton Syndrome: Implications for Mutation Detection and First Case of Prenatal Diagnosis

Journal of investigative dermatology, 2001-08, Vol.117 (2), p.179-187

2001

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Do Image Modality and Registration Method Influence the Accuracy of Craniofacial Navigation?

Journal of oral and maxillofacial surgery, 2012-09, Vol.70 (9), p.2165-2173

2012

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Antithrombotic Treatment in Neonatal Cerebral Sinovenous Thrombosis: Results of the International Pediatric Stroke Study

The Journal of pediatrics, 2010-05, Vol.156 (5), p.704-710.e2

2010

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Experimental flow studies in exact-replica phantoms of atherosclerotic carotid bifurcations under steady input conditions

Journal of biomechanical engineering, 2003-02, Vol.125 (1), p.38-48

2003

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Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

Journal of medical genetics, 2010-08, Vol.47 (8), p.513-524

2010

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Computer-Assisted Surgery in the Edentulous Jaw Based on 3 Fixed Intraoral Reference Points

Journal of oral and maxillofacial surgery, 2010-05, Vol.68 (5), p.1140-1147

2010

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Thymus Size at 6 Months of Age and Subsequent Child Mortality

The Journal of pediatrics, 2008-11, Vol.153 (5), p.683-688.e3

2008

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Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

Nature (London), 1989-11, Vol.342 (6247), p.238-243

1989

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Loss of Alleles from the Distal Short Arm of Chromosome 1 Occurs Late in Melanoma Tumor Progression

Proceedings of the National Academy of Sciences - PNAS, 1989-06, Vol.86 (12), p.4614-4618

1989

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Keratin 13 point mutation underlies the hereditary mucosal epithelia disorder white sponge nevus

Nature genetics, 1995-12, Vol.11 (4), p.453-455

1995

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Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

The New England journal of medicine, 1989-07, Vol.321 (4), p.213-218

1989

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Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma

A two-hit model for developmental defects in Gorlin syndrome

Mutation Hotspots Due to Sunlight in the p53 Gene of Nonmelanoma Skin Cancers

Randomized Multicenter Clinical Trial of Myofascial Physical Therapy in Women With Interstitial Cystitis/Painful Bladder Syndrome and Pelvic Floor Tenderness

Epidemiology of Congenital Cytomegalovirus Infection: Maternal Risk Factors and Molecular Analysis of Cytomegalovirus Strains

Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial

MPPH Syndrome: Two New Cases

Effect of Amitriptyline on Symptoms in Treatment Naïve Patients With Interstitial Cystitis/Painful Bladder Syndrome

Specialty care by child neurologists: a workforce analysis

Alfuzosin and Symptoms of Chronic Prostatitis–Chronic Pelvic Pain Syndrome

Errors and error management in image-guided craniomaxillofacial surgery

Relationship Between Sunlight Exposure and a Key Genetic Alteration in Basal Cell Carcinoma

Vitamin D receptor gene polymorphisms, serum 25-hydroxyvitamin D levels, and melanoma: UK case–control comparisons and a meta-analysis of published VDR data

Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the ovarian cancer association consortium pooled analysis

The Spectrum of Pathogenic Mutations in SPINK5 in 19 Families with Netherton Syndrome: Implications for Mutation Detection and First Case of Prenatal Diagnosis

Do Image Modality and Registration Method Influence the Accuracy of Craniofacial Navigation?

Antithrombotic Treatment in Neonatal Cerebral Sinovenous Thrombosis: Results of the International Pediatric Stroke Study

Experimental flow studies in exact-replica phantoms of atherosclerotic carotid bifurcations under steady input conditions

Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

Computer-Assisted Surgery in the Edentulous Jaw Based on 3 Fixed Intraoral Reference Points

Thymus Size at 6 Months of Age and Subsequent Child Mortality

Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

Loss of Alleles from the Distal Short Arm of Chromosome 1 Occurs Late in Melanoma Tumor Progression

Keratin 13 point mutation underlies the hereditary mucosal epithelia disorder white sponge nevus

Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

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