✦ LIBER ✦

TheMAPTH1 haplotype is associated with tangle-predominant dementia

✍ Scribed by Ismael Santa-Maria, Aya Haggiagi, Xinmin Liu, Jessica Wasserscheid, Peter T. Nelson, Ken Dewar, Lorraine N. Clark, John F. Crary

Book ID: 118783814
Publisher: Springer-Verlag
Year: 2012
Tongue: English
Weight: 726 KB
Volume: 124
Category: Article
ISSN: 0001-6322
DOI: 10.1007/s00401-012-1017-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Senile Dementia with Tangles (Tangle Pre

Senile Dementia with Tangles (Tangle Predominant Form of Senile Dementia)

✍ Kurt A. Jellinger; Christian Bancher 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 202 KB

Neurofibrillary tangle-predominant demen

Neurofibrillary tangle-predominant dementia: comparison with classical Alzheimer disease

✍ K. A. Jellinger; J. Attems 📂 Article 📅 2006 🏛 Springer-Verlag 🌐 English ⚖ 667 KB

The H2 MAPT haplotype is associated with

The H2 MAPT haplotype is associated with familial frontotemporal dementia

✍ Roberta Ghidoni; Simona Signorini; Laura Barbiero; Elena Sina; Paola Cominelli; 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 116 KB

Tangle-only dementia is associated with

Tangle-only dementia is associated with variation in the MAPT 3' UTR

✍ Santa-Maria, Ismael; Haggiagi, Aya; Alaniz, Maria Eugenia; Liu, Xinmin; Vonsatte 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 60 KB

MAPT H1 haplotype is associated with enh

MAPT H1 haplotype is associated with enhanced α-synuclein deposition in dementia with Lewy bodies

✍ Martí Colom-Cadena; Ellen Gelpi; María J. Martí; Sara Charif; Oriol Dols-Icardo; 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 593 KB

The codon 408 mutation associated with h

The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria

✍ Jadwiga Jaruzelska; Karen Friis Henriksen; Flemming Güttler; Olaf Riess; Krzyszt 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 382 KB

The incidence of phenylketonuria (PKU) in the western part of Poland is 1 in 5000 live births. Restriction fragment length polymorphism (RFLP) haplotypes at the phenylalanine hydroxylase locus have been analysed in 46 Polish families with PKU. Among 43 fully-informative families 16 RFLP haplotypes w