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KOREY ULLRICH, M.D.
M.D.
Rheumatology Physician
NPI: 1639342124Individual
Specialties, Licenses & Credentials
Rheumatology PhysicianPrimary
Internal Medicine — Rheumatology
Code: 207RR0500X
ME109362(FL)
Research & Publications (20)
Seroepidemiological study in a Puumala virus outbreak area in South-East Germany.
PMID 19148676·Med Microbiol Immunol·2009
4-observational
Phenylalanine tolerance in three phenylketonuric women pregnant with fetuses of different genetic PKU status.
PMID 19194782·J Inherit Metab Dis·2009
5-case
[Long-term school-development of children with impaired language skills: 15-years follow up after dismissal from child care centres with speech therapy].
PMID 19554501·Laryngorhinootologie·2009
8-other
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship.
PMID 19309691·Hum Mutat·2009
5-case
GAR22: a novel target gene of thyroid hormone receptor causes growth inhibition in human erythroid cells.
PMID 19375645·Exp Hematol·2009
8-other
High concentrations of phenylalanine stimulate peroxisome proliferator-activated receptor gamma: implications for the pathophysiology of phenylketonuria.
PMID 18755275·Neurobiol Dis·2008
8-other
Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1.
PMID 18348873·Biochim Biophys Acta·2008
7-preclinical
Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH).
PMID 18775954·Hum Mol Genet·2008
4-observational
Abeta-globulomers are formed independently of the fibril pathway.
PMID 18353662·Neurobiol Dis·2008
4-observational
Membrane translocation of glutaric acid and its derivatives.
PMID 18404412·J Inherit Metab Dis·2008
6-review
MRI abnormalities in normal-appearing brain tissue of treated adult PKU patients.
PMID 18425822·J Magn Reson Imaging·2008
8-other
The mutation p.Ser298Pro in the sulphamidase gene (SGSH) is associated with a slowly progressive clinical phenotype in mucopolysaccharidosis type IIIA (Sanfilippo A syndrome).
PMID 18407553·Hum Mutat·2008
8-other
Reduced cerebral fluoro-L-dopamine uptake in adult patients suffering from phenylketonuria.
PMID 17971791·J Cereb Blood Flow Metab·2008
8-other
Identification of molecular compounds critical to Alzheimer's-like plaque formation.
PMID 17492785·J Neurosci Res·2007
8-other
Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A).
PMID 17938166·Pediatrics·2007
4-observational
3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3.
PMID 17356845·J Mol Med (Berl)·2007
7-preclinical
Cannabinoid 1 (CB1) receptors coupled to cholinergic motorneurones inhibit neurogenic circular muscle contractility in the human colon.
PMID 16520743·Br J Pharmacol·2006
8-other
Elevated phenylalanine levels interfere with neurite outgrowth stimulated by the neuronal cell adhesion molecule L1 in vitro.
PMID 16716305·FEBS Lett·2006
7-preclinical
Alzheimer-like plaque formation by human macrophages is reduced by fibrillation inhibitors and lovastatin.
PMID 16765377·J Mol Biol·2006
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
- 1050 NW 15TH ST, SUITE 208A
BOCA RATON, FL 33486 - Phone
- (561) 368-2125
Quick Facts
- NPI
- 1639342124
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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