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PATRICK WATERS, PHARM.D.
PHARM.D.
Pharmacotherapy Pharmacist
NPI: 1205941200Individual
Specialties, Licenses & Credentials
Pharmacotherapy PharmacistPrimary
Pharmacist — Pharmacotherapy
Code: 1835P1200X
5302025189(MI)
Research & Publications (20)
Surgical treatment of carpal and hand injuries in children.
PMID 18399606·Instr Course Lect·2008
6-review
The early effects of tendon transfers and open capsulorrhaphy on glenohumeral deformity in brachial plexus birth palsy.
PMID 18829915·J Bone Joint Surg Am·2008
8-other
Forearm rebalancing in osteochondromatosis by radioulnar fusion.
PMID 18090828·Tech Hand Up Extrem Surg·2007
8-other
The effect of derotational humeral osteotomy on global shoulder function in brachial plexus birth palsy.
PMID 16651578·J Bone Joint Surg Am·2006
8-other
Update on management of pediatric brachial plexus palsy.
PMID 15931025·J Pediatr Orthop B·2005
6-review
Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: a unique patient or a novel metabolic disorder?
PMID 16182582·Mol Genet Metab·2005
5-case
Effect of tendon transfers and extra-articular soft-tissue balancing on glenohumeral development in brachial plexus birth palsy.
PMID 15687154·J Bone Joint Surg Am·2005
8-other
Interobserver and intraobserver reliability of therapist-assisted videotaped evaluations of upper-limb hemiplegia.
PMID 15043910·J Hand Surg Am·2004
8-other
How PAH gene mutations cause hyper-phenylalaninemia and why mechanism matters: insights from in vitro expression.
PMID 12655545·Hum Mutat·2003
6-review
Surgical treatment of nonunion and avascular necrosis of the proximal part of the scaphoid in adolescents.
PMID 12063324·J Bone Joint Surg Am·2002
8-other
Degradation of mutant proteins, underlying "loss of function" phenotypes, plays a major role in genetic disease.
PMID 11488412·Curr Issues Mol Biol·2001
6-review
Homomeric and heteromeric interactions between wild-type and mutant phenylalanine hydroxylase subunits: evaluation of two-hybrid approaches for functional analysis of mutations causing hyperphenylalaninemia.
PMID 11461190·Mol Genet Metab·2001
8-other
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotype.
PMID 10720436·Mol Genet Metab·2000
8-other
Investigations of HPA function and the enduring consequences of stressors in adolescence in animal models.
PMID 19616355·Brain Cogn·2010
6-review
Salvage reconstruction of congenital pseudarthrosis of the clavicle with vascularized fibular graft after failed operative treatment: a case report.
PMID 19461387·J Pediatr Orthop·2009
5-case
Changes in hyporesponsiveness to acute amphetamine and age differences in tyrosine hydroxylase immunoreactivity in the brain over adolescence in male and female rats.
PMID 19492363·Dev Psychobiol·2009
7-preclinical
Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplification.
PMID 19501531·Mol Genet Metab·2009
8-other
Brain abnormalities in Sjogren syndrome with recurrent CNS manifestations: association with neuromyelitis optica.
PMID 19625331·Mult Scler·2009
8-other
Symptomatic, radiological and pathological involvement of the hypothalamus in neuromyelitis optica.
PMID 19448094·J Neurol Neurosurg Psychiatry·2009
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 820 S DAMEN AVE
CHICAGO, IL 60612 - Phone
- (312) 569-7932
Quick Facts
- NPI
- 1205941200
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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