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JANE KUNZE, PHD
PHD
Clinical Neuropsychologist
NPI: 1306965272Individual
Specialties, Licenses & Credentials
Clinical NeuropsychologistPrimary
Clinical Neuropsychologist
Code: 103G00000X
03203(MD)
Research & Publications (20)
In situ PM-IRRAS studies of an archaea analogue thiolipid assembled on a au(111) electrode surface.
PMID 19499931·Langmuir·2009
8-other
Photo-induced effects on self-organized TiO2 nanotube arrays: the influence of surface morphology.
PMID 19417323·Nanotechnology·2009
8-other
[Cutaneous malignant peripheral nerve sheath tumor in neurofibromatosis type 1].
PMID 19221702·Hautarzt·2009
5-case
TiO2 nanotubes in dye-sensitized solar cells: critical factors for the conversion efficiency.
PMID 19197925·Chem Asian J·2009
8-other
Corrosion resistance studies on grain-boundary etched drug-eluting stents.
PMID 17277971·J Mater Sci Mater Med·2007
8-other
New method to measure packing densities of self-assembled thiolipid monolayers.
PMID 16732685·Langmuir·2006
8-other
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
PMID 15340364·Eur J Hum Genet·2004
8-other
Symmetry is in the eye of the beeholder: innate preference for bilateral symmetry in flower-naïve bumblebees.
PMID 15278213·Naturwissenschaften·2004
7-preclinical
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene.
PMID 15200508·Clin Genet·2004
5-case
Spondyloepiphyseal dysplasia Omani type: a new recessive type of SED with progressive spinal involvement.
PMID 15098240·Am J Med Genet A·2004
8-other
Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.
PMID 14695538·Hum Mutat·2004
8-other
Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes.
PMID 14571271·Eur J Hum Genet·2003
8-other
Survival to adulthood and dominant inheritance of platyspondylic skeletal dysplasia, Torrance-Luton type.
PMID 12961049·Pediatr Radiol·2003
5-case
Congenital generalized lipodystrophy, mental retardation, deafness, short stature, and slender bones: a newly recognized syndrome?
PMID 12923870·Am J Med Genet A·2003
5-case
Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation.
PMID 12905014·Eur J Pediatr·2003
5-case
Cerebral manifestations, hemihypertrophy and lymphoedema of one leg in a child with epidermal nevus syndrome (Schimmelpenning-Feuerstein-Mims).
PMID 12802536·Pediatr Radiol·2003
5-case
Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.
PMID 12599186·Am J Med Genet A·2003
5-case
Autosomal recessive type of Adams-Oliver syndrome: prenatal diagnosis.
PMID 12423491·Ultrasound Obstet Gynecol·2002
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
- 707 N BROADWAY
BALTIMORE, MD 21205 - Phone
- (443) 923-1886
Quick Facts
- NPI
- 1306965272
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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