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PAUL WATERS, M.D.
M.D.
Thoracic Surgery (Cardiothoracic Vascular Surgery) Physician
NPI: 1811955958Individual
Specialties, Licenses & Credentials
Thoracic Surgery (Cardiothoracic Vascular Surgery) PhysicianPrimary
Thoracic Surgery (Cardiothoracic Vascular Surgery)
Code: 208G00000X
040613(CT)
Research & Publications (20)
Mammalian sex--Origin and evolution of the Y chromosome and SRY.
PMID 17400006·Semin Cell Dev Biol·2007
6-review
Autosomal location of genes from the conserved mammalian X in the platypus (Ornithorhynchus anatinus): implications for mammalian sex chromosome evolution.
PMID 15973504·Chromosome Res·2005
7-preclinical
The human Y chromosome derives largely from a single autosomal region added to the sex chromosomes 80-130 million years ago.
PMID 11306800·Cytogenet Cell Genet·2001
4-observational
Investigations of HPA function and the enduring consequences of stressors in adolescence in animal models.
PMID 19616355·Brain Cogn·2010
6-review
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
Does the human X contain a third evolutionary block? Origin of genes on human Xp11 and Xq28.
PMID 19439513·Genome Res·2009
7-preclinical
Brain abnormalities in Sjogren syndrome with recurrent CNS manifestations: association with neuromyelitis optica.
PMID 19625331·Mult Scler·2009
8-other
Therapeutic effects of recombinant forms of full-length and truncated human surfactant protein D in a murine model of invasive pulmonary aspergillosis.
PMID 19403176·Mol Immunol·2009
7-preclinical
Patient and staff perspective of a nurse-led support programme for patients waiting for cardiac surgery: participant perspective of a cardiac support programme.
PMID 18504160·Eur J Cardiovasc Nurs·2009
8-other
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations.
PMID 19217814·Mol Genet Metab·2009
8-other
Folinic acid-responsive seizures are identical to pyridoxine-dependent epilepsy.
PMID 19142996·Ann Neurol·2009
5-case
Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family.
PMID 19062322·Mol Genet Metab·2009
7-preclinical
Symptomatic, radiological and pathological involvement of the hypothalamus in neuromyelitis optica.
PMID 19448094·J Neurol Neurosurg Psychiatry·2009
5-case
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
Conservation of a chromosome arm in two distantly related marsupial species.
PMID 19420927·Cytogenet Genome Res·2009
7-preclinical
Progressive encephalomyelitis, rigidity, and myoclonus: a novel glycine receptor antibody.
PMID 18852446·Neurology·2008
5-case
Physical map of two tammar wallaby chromosomes: a strategy for mapping in non-model mammals.
PMID 18987984·Chromosome Res·2008
4-observational
Antibody to aquaporin-4 in the long-term course of neuromyelitis optica.
PMID 18945724·Brain·2008
8-other
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 77 LAFAYETTE PL, SUITE 302
GREENWICH, CT 06830 - Phone
- (203) 868-4341
Quick Facts
- NPI
- 1811955958
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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