NeilRFriedmanMD

Child Neurology • Phoenix, AZ

Director, Barrow Neurological Institute, Phoenix Children's

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Office
1919 E. Thomas Roaad
Phoenix, AZ 85016
Phone+1 602-933-0970

Fax+1 602-933-4253

Education & Training

Boston Children’s Hospital/Beth Israel Deaconess Medical Center/Harvard Medical SchoolFellowship, Child Neurology, 1995 - 1998
University of Arizona College of Medicine-TucsonResidency, Pediatrics, 1993 - 1995
University of Cape Town Faculty of MedicineClass of 1987

Certifications & Licensure

AZ State Medical License 2019 - 2026
OH State Medical License 1998 - 2025
American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology

Awards, Honors, & Recognition

Best Doctors Best Doctors, Inc.
CMS Meaningful Use Stage 1 Certification EpicCare Ambulatory EMR, Epic Systems Corporation, 2011
Top MD Consumers Checkbook

Clinical Trials

Assess Specific Kinds of Children Challenges for Neurologic Devices Study Start of enrollment: 2009 Mar 01
Terminated
Safety Study of 3 mg/mL Baclofen Injection (Intrathecal) Using A Programmable Pump Start of enrollment: 2012 Dec 01
Completed
Phase 3

Publications & Presentations

PubMed

403 citations
Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe, Sumit Parikh, Neil R. Friedman
The New England Journal of Medicine. 2012-10-03
238 citations
Predictors of cerebral arteriopathy in children with arterial ischemic stroke: results of the International Pediatric Stroke Study.
Catherine Amlie-Lefond, Timothy J. Bernard, Guillaume Sébire, Neil R. Friedman, Geoffrey L. Heyer
Circulation. 2009-03-17
8 citations
'Double trouble': diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia.
Sandra Donkervoort, Alice B. Schindler, Carolina Tesi-Rocha, Allison Schreiber, M. Leach
Neuromuscular Disorders. 2013-12-01

Press Mentions

Deletion of Conserved Non‐Coding Sequences Downstream from NKX2‐1: A Novel Disease‐Causing Mechanism for Benign Hereditary ChoreaMarch 5th, 2021