Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 3 (of 3 Records)

Query Trace: Neuroferritinopathy[original query]
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.
Journal of human genetics 2006 51 (8): 645-51.
Costa Maria do Carmo, Teixeira-Castro Andreia, Constante Marco, Magalhães Marina, Magalhães Paula, Cerqueira Joana, Vale José, Passão Vitorina, Barbosa Célia, Robalo Conceição, Coutinho Paula, Barros José, Santos Manuela M, Sequeiros Jorge, Maciel Patríc
Analysis of ferritin genes in Parkinson disease.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2007 45 (11): 1450-6.
Foglieni Barbara, Ferrari Francesca, Goldwurm Stefano, Santambrogio Paolo, Castiglioni Emanuela, Sessa Maria, Volontè Maria Antonietta, Lalli Stefania, Galli Carlo, Wang Xin-Sheng, Connor James, Sironi Francesca, Canesi Margherita, Biasiotto Giorgio, Pezzoli Gianni, Levi Sonia, Ferrari Maurizio, Arosio Paolo, Cremonesi Lau
Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.
Genetic testing and molecular biomarkers 2010 Dec 14 (6): 793-6.
Castiglioni Emanuela, Finazzi Dario, Goldwurm Stefano, Levi Sonia, Pezzoli Gianni, Garavaglia Barbara, Nardocci Nardo, Malcovati Luca, Porta Matteo G Della, Gallì Anna, Forni Gian Luca, Girelli Domenico, Maccarinelli Federica, Poli Maura, Ferrari Maurizio, Cremonesi Laura, Arosio Pao
TOP