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Longitudinal change in basal ganglia volume in patients with Huntington's disease

Neurology, 1997-02, Vol.48 (2), p.394-399

1997

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Frontal lobe volume in patients with Huntington's disease

Neurology, 1998-01, Vol.50 (1), p.252-258

1998

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Familial influence on age of onset among siblings with Huntington disease

American journal of medical genetics, 2001-07, Vol.105 (5), p.399-403

2001

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Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees

Movement disorders, 1997-07, Vol.12 (4), p.519-530

1997

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A controlled trial of idebenone in Huntington's disease

Movement disorders, 1996-09, Vol.11 (5), p.549-554

1996

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Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Nature genetics, 1999-12, Vol.23 (4), p.391-392

1999

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Two Novel Single–Base-Pair Substitutions Adjacent to the CAG Repeat in the Huntington Disease Gene (IT15): Implications for Diagnostic Testing

American journal of human genetics, 1999, Vol.64 (1), p.323-325

1999

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Does CAG repeat number predict the rate of pathological changes in Huntington's disease?

Annals of neurology, 1998-10, Vol.44 (4), p.708-709

1998

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Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease

Movement disorders, 2000-05, Vol.15 (3), p.552-560

2000

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Unified Huntington's disease rating scale: Reliability and consistency

Movement disorders, 1996-03, Vol.11 (2), p.136-142

1996

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Innovative Service or Proselytizing: Exploring When Services Delivery Becomes a Platform for Unwanted Religious Persuasion

Social work (New York), 2009-04, Vol.54 (2), p.157-165

2009

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Patients with features similar to Huntington's disease, without CAG expansion in huntingtin

Neurology, 1998-07, Vol.51 (1), p.215-220

1998

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Bayesian Analysis for Evidence-based Practice in Social Work

Social work research, 2011-03, Vol.35 (1), p.46-52

2011

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Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expression

Journal of medical genetics, 1999-01, Vol.36 (1), p.62-64

1999

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Anticipation and instability of IT-15 (CAG)N repeats in parent-offspring pairs with Huntington disease

American journal of human genetics, 1995-09, Vol.57 (3), p.593-602

1995

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Improvement of Psychiatric Symptoms in Youth Following Resolution of Sinusitis

International journal of pediatric otorhinolaryngology, 2017-01, Vol.92, p.38-44

2017

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Metadata tables to enable dynamic data modeling and web interface design: the SEER example

International journal of medical informatics (Shannon, Ireland), 2002-04, Vol.65 (1), p.51-58

2002

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Mitigating DoS attack through selective bin verification

1st IEEE ICNP Workshop on Secure Network Protocols, 2005. (NPSec), 2005, p.7-12

2005

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Laterality of Brain and Ocular Lesions in Aicardi Syndrome

Pediatric neurology, 2011-09, Vol.45 (3), p.149-154

2011

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Evidence-Based Risk Management: How Can We Succeed?: Deliberations from a Risk Management Advisory Council

Drug information journal, 2003-01, Vol.37 (1), p.127-134

2003

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Dilated Perivascular Spaces: An Informative Radiologic Finding in Sanfilippo Syndrome Type A

Pediatric neurology, 2008-05, Vol.38 (5), p.363-366

2008

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Experimental Results Toward the Customization of Information Systems

Human relations (New York), 1986-02, Vol.39 (2), p.117-134

1986

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Diffusion Tensor Imaging of Aicardi Syndrome

Pediatric neurology, 2010-08, Vol.43 (2), p.87-91

2010

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Introduction

Seminars in pediatric neurology, 2009, Vol.16 (3), p.99-100

Sherr, Elliott H., MD, PhD

2009

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Broadening the Scope of the Rehabilitation Act of 1973

Nursing management, 1997-06, Vol.28 (6), p.41-42

1997

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Longitudinal change in basal ganglia volume in patients with Huntington's disease

Frontal lobe volume in patients with Huntington's disease

Familial influence on age of onset among siblings with Huntington disease

Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees

A controlled trial of idebenone in Huntington's disease

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Two Novel Single–Base-Pair Substitutions Adjacent to the CAG Repeat in the Huntington Disease Gene (IT15): Implications for Diagnostic Testing

Does CAG repeat number predict the rate of pathological changes in Huntington's disease?

Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease

Unified Huntington's disease rating scale: Reliability and consistency

Innovative Service or Proselytizing: Exploring When Services Delivery Becomes a Platform for Unwanted Religious Persuasion

Patients with features similar to Huntington's disease, without CAG expansion in huntingtin

Bayesian Analysis for Evidence-based Practice in Social Work

Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expression

Anticipation and instability of IT-15 (CAG)N repeats in parent-offspring pairs with Huntington disease

Improvement of Psychiatric Symptoms in Youth Following Resolution of Sinusitis

Metadata tables to enable dynamic data modeling and web interface design: the SEER example

Mitigating DoS attack through selective bin verification

Laterality of Brain and Ocular Lesions in Aicardi Syndrome

Evidence-Based Risk Management: How Can We Succeed?: Deliberations from a Risk Management Advisory Council

Dilated Perivascular Spaces: An Informative Radiologic Finding in Sanfilippo Syndrome Type A

Experimental Results Toward the Customization of Information Systems

Diffusion Tensor Imaging of Aicardi Syndrome

Introduction

Broadening the Scope of the Rehabilitation Act of 1973

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