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DR. CHRISTINE HANNA ELISABETH BERGMANN M.D., PH.D.
M.D., PH.D.
Neurology Physician
NPI: 1528157450Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
043622(CT)
Research & Publications (20)
Cardiac risk factors and potential treatments in Alzheimer's disease.
PMID 16945210·Neurol Res·2006
6-review
CD40L gene transfer in immunotherapy of cancer: more than co-stimulation?
PMID 19106641·Cancer Biol Ther·2009
8-other
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.
PMID 18371931·Am J Hum Genet·2008
7-preclinical
Functional analysis of PKHD1 splicing in autosomal recessive polycystic kidney disease.
PMID 16897190·J Hum Genet·2006
5-case
Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
PMID 17186469·Am J Hum Genet·2006
8-other
Arteriogenesis depends on circulating monocytes and macrophage accumulation and is severely depressed in op/op mice.
PMID 16684892·J Leukoc Biol·2006
7-preclinical
Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease.
PMID 16771602·Mol Diagn Ther·2006
6-review
Quality of pronase dissociation of mature inferior colliculus neurons.
PMID 15965702·Eur Arch Otorhinolaryngol·2005
8-other
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD).
PMID 16199545·J Med Genet·2005
8-other
Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD).
PMID 15698423·Kidney Int·2005
8-other
Algorithm for efficient PKHD1 mutation screening in autosomal recessive polycystic kidney disease (ARPKD).
PMID 15706593·Hum Mutat·2005
6-review
Analysis of splice donor and acceptor function in a novel Ac-based gene trap construct.
PMID 15173944·Planta·2004
8-other
PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD).
PMID 15108281·Hum Mutat·2004
8-other
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).
PMID 15108277·Hum Mutat·2004
6-review
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).
PMID 12506140·J Am Soc Nephrol·2003
8-other
Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC).
PMID 12910495·Am J Med Genet A·2003
6-review
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia.
PMID 12805098·Brain·2003
5-case
Allelic variants in the 5' non-coding region of the connexin32 gene: possible pitfalls in the diagnosis of X linked Charcot-Marie-Tooth neuropathy (CMTX).
PMID 12205128·J Med Genet·2002
8-other
Th1 or Th2: how an appropriate T helper response can be made.
PMID 11374299·Bull Math Biol·2001
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 130 W KINGSBRIDGE ROAD
BRONX, NY 10468 - Phone
- (718) 584-9000
Quick Facts
- NPI
- 1528157450
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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