✦ LIBER ✦

Analysis of phenotypic variation in psoriasis as a function of age at onset and family history

✍ Scribed by Philip Stuart; Farah Malick; Rajan P. Nair; Tilo Henseler; Henry W. Lim; Stefan Jenisch; John Voorhees; Enno Christophers; James T. Elder

Publisher: Springer-Verlag
Year: 2002
Tongue: English
Weight: 54 KB
Volume: 294
Category: Article
ISSN: 0340-3696
DOI: 10.1007/s00403-002-0321-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Age of onset, age at examination, and ot

Age of onset, age at examination, and other covariates in the analysis of family data

✍ Dr. R. C. Elston; V. T. George 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB

Information on age of onset can easily be incorporated into regressive logistic models by assuming that age of onset follows a logistic distribution. This is analogous to previously proposed models based on the normal distribution. The two distributions, and hence the two types of models, are very s

Family history and age at onset of breas

Family history and age at onset of breast cancer in Hispanic and non-Hispanic white women

✍ Betsy Risendal; Lisa M. Hines; Carol Sweeney; Martha L. Slattery; Anna R. Giulia 📂 Article 📅 2008 🏛 Springer Netherlands 🌐 English ⚖ 168 KB

Family and molecular data for a fine ana

Family and molecular data for a fine analysis of age at onset in Huntington disease

✍ Squitieri, F. ;Sabbadini, G. ;Mandich, P. ;Gellera, C. ;Di Maria, E. ;Bellone, E 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 138 KB 👁 2 views

We analyzed the data on age at onset and CAG size of 319 patients clinically diagnosed with Huntington disease (HD) and 86 presymptomatic subjects recorded by four Italian Centers over the last 14 years. To overcome the problem of different CAG numbers found in each subject, also in the same family,

Marked variation in clinical presentatio

Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation

✍ Louis C. Tan; Caroline M. Tanner; Rong Chen; Piu Chan; Matthew Farrer; John Hard 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 66 KB

## Abstract Parkin gene mutations have been detected in families with early‐onset autosomal recessive parkinsonism. We report a novel heterozygous 40 base pair deletion in exon 3 of the parkin gene that increases the susceptibility of carriers to develop parkinsonism/dystonia and manifests remarkab

Diurnal variation in hepatic glutathione

Diurnal variation in hepatic glutathione content as a function of age

✍ Dr. Lora E. Rikans; Munetaka Nokubo; Setsuko Kanai; Kenichi Kitani 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 325 KB

Assessment of association of D3 dopamine

Assessment of association of D3 dopamine receptorMscI polymorphism with schizophrenia: Analysis of symptom ratings, family history, age at onset, and movement disorders

✍ Gaitonde, E. J.; Morris, A.; Sivagnanasundaram, S.; McKenna, P. J.; Hunt, D. M.; 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 462 KB 👁 2 views

Several studies have reported an association between schizophrenia and homozygosity for the MscI restriction site in exon 1 of the D3 dopamine receptor gene, but other studies have failed to find this association. Recent reports have suggested that the association is most salient in male patients wi