La maladie de Parkinson en France (serveur d'exploration) - Checkpoint (Istex)

Index « Titre (en) » - entrée « family »
Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.
families < family < famous  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 8.
Ident.Authors (with country if any)Title
000180 (2012) David Michael Weekes ; Nathalie Baradel ; Nathalie Kyritsakas [France] ; Pierre Mobian [France] ; Marc Henry [France]Rational Synthesis of a Family of Neutral Monomeric Heteroleptic Titanium Complexes Based on an Octahedral TiO4N2 Motif
000A26 (2006) Shannon K. Mcdonnell [États-Unis] ; Daniel J. Schaid [États-Unis] ; Alexis Elbaz [États-Unis, France] ; Kari J. Strain [États-Unis] ; James H. Bower [États-Unis] ; J. Eric Ahlskog [États-Unis] ; Demetrius M. Maraganore [États-Unis] ; Walter A. Rocca [États-Unis]Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study
000A67 (2005) Bao Ton-Hoang [France] ; Catherine Guynet [France] ; Donald R. Ronning [États-Unis] ; Brigitte Cointin-Marty [France] ; Fred Dyda [États-Unis] ; Michael Chandler [France]Transposition of ISHp608, member of an unusual family of bacterial insertion sequences
000B13 (2005) Abdelaziz Tlili [Tunisie] ; Ilhem Charfedine [Tunisie] ; Imed Lahmar [Tunisie] ; Zaineb Benzina [Tunisie] ; Ben Amor Mohamed [Tunisie] ; Dominique Weil [France] ; Nabil Idriss [Tunisie] ; Mohamed Drira [Tunisie] ; Saber Masmoudi [Tunisie] ; Hammadi Ayadi [Tunisie]Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non‐syndromic recessive hearing loss
001153 (2000) Stellan Mörner [Suède] ; Pascale Richard [France] ; Elsadig Kazzam [Suède] ; Bernard Hainque [France] ; Ketty Schwartz [France] ; Anders Waldenström [Suède]Deletion in the Cardiac Troponin I Gene in a Family From Northern Sweden with Hypertrophic Cardiomyopathy
001512 (1998) Johann Tassin ; Alexandra Dürr ; Thomas De Broucker [France] ; Nacer Abbas ; Vincenzo Bonifati ; Giuseppe De Michele ; Anne-Marie Bonnet ; Emmanuel Broussolle ; Pierre Pollak [France] ; Marie Vidailhet ; Michele De Mari [Italie] ; Roberto Marconi [Italie] ; Soraya Medjbeur ; Allessandro Filla ; Giuseppe Meco ; Yves Agid [France] ; Alexis Brice [France]Chromosome 6–Linked Autosomal Recessive Early-Onset Parkinsonism: Linkage in European and Algerian Families, Extension of the Clinical Spectrum, and Evidence of a Small Homozygous Deletion in One Family
001A64 (1994) François Berthou [France] ; Yvonne Dreano [France] ; Claire Belloc [Finlande] ; Lauri Kangas [France] ; Jean-Charles Gautier [Finlande] ; Philippe Beaune [Finlande]Involvement of cytochrome P450 3A enzyme family in the major metabolic pathways of toremifene in human liver microsomes
001D79 (1991) Françoise Jacolot [France] ; Isabelle Simon [France] ; Yvonne Dreano [France] ; Philippe Beaune [France] ; Christian Riche [France] ; François Berthou [France]Identification of the cytochrome P450 IIIA family as the enzymes involved in the N-demethylation of tamoxifen in human liver microsomes

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonFranceV1/Data/Istex/Checkpoint
HfdIndexSelect -h $EXPLOR_AREA/Data/Istex/Checkpoint/Title.i -k "family" 
HfdIndexSelect -h $EXPLOR_AREA/Data/Istex/Checkpoint/Title.i  \
                -Sk "family" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Istex/Checkpoint/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    ParkinsonFranceV1
   |flux=    Istex
   |étape=   Checkpoint
   |type=    indexItem
   |index=    Title.i
   |clé=    family
}}

Wicri

This area was generated with Dilib version V0.6.29.
Data generation: Wed May 17 19:46:39 2017. Site generation: Mon Mar 4 15:48:15 2024