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INGE MEIJER, MD, PHD
MD, PHD
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1629452685Individual
Specialties, Licenses & Credentials
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
P97342(NY)
Research & Publications (19)
Angiomotin-like protein 1 controls endothelial polarity and junction stability during sprouting angiogenesis.
PMID 19590046·Circ Res·2009
7-preclinical
ErbB2 and ErbB4 Cbl binding sites can functionally replace the ErbB1 Cbl binding site.
PMID 19263517·Cell Signal·2009
7-preclinical
A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.
PMID 19001169·Arch Neurol·2008
8-other
Wnt signaling acts and is regulated in a human osteoblast differentiation dependent manner.
PMID 18186078·J Cell Biochem·2008
8-other
CSCI/RCPSC Henry Friesen lecture: the past and the future of neurogenetics.
PMID 18053395·Clin Invest Med·2007
8-other
Effect of virtual articulator settings on occlusal morphology of CAD/CAM restorations.
PMID 17899892·Int J Comput Dent·2007
8-other
SPG4 founder effect in French Canadians with hereditary spastic paraplegia.
PMID 17598600·Can J Neurol Sci·2007
8-other
A stop codon mutation in SCN9A causes lack of pain sensation.
PMID 17597096·Hum Mol Genet·2007
7-preclinical
Characterization of a novel SPG3A deletion in a French-Canadian family.
PMID 17427918·Ann Neurol·2007
8-other
Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.
PMID 17345589·Hum Mutat·2007
8-other
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
PMID 17160902·Am J Hum Genet·2007
7-preclinical
A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors.
PMID 16175507·Am J Hum Genet·2005
8-other
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice.
PMID 15755680·Neurobiol Dis·2005
4-observational
A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy.
PMID 15523628·Am J Med Genet A·2004
8-other
A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
PMID 15455396·Ann Neurol·2004
4-observational
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred.
PMID 12509863·Ann Neurol·2003
8-other
Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.
PMID 11843700·Arch Neurol·2002
8-other
A locus for autosomal dominant hereditary spastic ataxia, SAX1, maps to chromosome 12p13.
PMID 11774073·Am J Hum Genet·2002
8-other
Transcriptional regulation of human papillomavirus type 16 LCR by different C/EBPbeta isoforms.
PMID 10820487·Mol Carcinog·2000
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
- 10 UNION SQ E FL 5, SUITE 5K
NEW YORK, NY 10003 - Phone
- (212) 844-6050
Quick Facts
- NPI
- 1629452685
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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