La psychogénéalogie : À la recherche des racines familiales de la maladieROOBAERT, V.Louvain médical. 2006, Vol 125, Num 7, pp 245-251, issn 0024-6956, 7 p.Article

Molecular genetics of adrenocortical tumours, from familial to sporadic diseasesLIBE, Rossella; BERTHERAT, Jérome.European journal of endocrinology. 2005, Vol 153, Num 4, pp 477-487, issn 0804-4643, 11 p.Article

Forme familiale bénigne de maladie de Degos = Benign familial Degos diseasePINAULT, A.-L; BARBAUD, A; WEBER-MULLER, F et al.Annales de dermatologie et de vénéréologie. 2004, Vol 131, Num 11, pp 989-993, issn 0151-9638, 5 p.Article

A Clinical Characterization of Familial Keloid Disease in Unique African Tribes Reveals Distinct Keloid PhenotypesBELLA, Husam; HEISE, Marco; YAGI, Khalid I et al.Plastic and reconstructive surgery (1963). 2011, Vol 127, Num 2, pp 689-702, issn 0032-1052, 14 p.Article

The pattern of atrophy in familial Alzheimer disease: Volumetric MRI results from the DIAN studyCASH, David M; RIDGWAY, Gerard R; GHETTI, Bernardino F et al.Neurology. 2013, Vol 81, Num 16, pp 1425-1433, issn 0028-3878, 9 p.Article

Early detection of familial Creutzfeldt Jakob disease on diffusion-weighted imaging before symptom onsetTERASAWA, Yuka; FUJITA, Koji; IZUMI, Yuishin et al.Journal of the neurological sciences. 2012, Vol 319, Num 1-2, pp 130-132, issn 0022-510X, 3 p.Article

Early-Onset Familial Alzheimer's Disease (EOFAD)LIYONG WU; ROSA-NETO, Pedro; HSIUNG, Ging-Yuek R et al.Canadian journal of neurological sciences. 2012, Vol 39, Num 4, pp 436-445, issn 0317-1671, 10 p.Article

Evidence for Premature Lipid Raft Aging in APP/PS1 Double-Transgenic Mice, a Model of Familial Alzheimer DiseaseFABELO, Noemi; MARTIN, Virginia; MARIN, Raquel et al.Journal of neuropathology and experimental neurology. 2012, Vol 71, Num 10, pp 868-881, issn 0022-3069, 14 p.Article

High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern NewfoundlandMAHONEY, Krista; BUCKLEY, David; ALAM, Muhammed et al.Epilepsy research. 2012, Vol 98, Num 2-3, pp 140-147, issn 0920-1211, 8 p.Article

Clinical Course of Patients with Familial Early-Onset Alzheimer's Disease Potentially Lacking Senile Plaques Bearing the E693Δ Mutation in Amyloid Precursor ProteinSHIMADA, Hiroyuki; ATAKA, Suzuka; TOMIYAMA, Takami et al.Dementia and geriatric cognitive disorders. 2011, Vol 32, Num 1, pp 45-54, issn 1420-8008, 10 p.Article

Familial Thoracic Aortic Aneurysms and Dissections: Identification of a Novel Locus for Stable Aneurysms With a Low Risk for Progression to Aortic DissectionGUO, Dong-Chuan; REGALADO, Ellen S; SHETE, Sanjay S et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 1, pp 36-42, issn 1942-325X, 7 p.Article

Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical PhenotypePROBST, Susanne; OECHSLIN, Erwin; SCHULER, Pia et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 4, pp 367-374, issn 1942-325X, 8 p.Article

The ALS8-associated mutant VAPB^P56S is resistant to proteolysis in neuronsGKOGKAS, Christos; WARDROPE, Caroline; HANNAH, Matthew et al.Journal of neurochemistry. 2011, Vol 117, Num 2, pp 286-294, issn 0022-3042, 9 p.Article

Presenilin-1 but not amyloid precursor protein mutations present in mouse models of Alzheimer's disease attenuate the response of cultured cells to γ-secretase modulators regardless of their potency and structureHAHN, Stefanie; BRÜNING, Tanja; NESS, Julia et al.Journal of neurochemistry. 2011, Vol 116, Num 3, pp 385-395, issn 0022-3042, 11 p.Article

Role of presenilin1 in structural plasticity of cortical dendritic spines in vivoJUNG, Christian K. E; FUHRMANN, Martin; HONARNEJAD, Kamran et al.Journal of neurochemistry. 2011, Vol 119, Num 5-6, pp 1064-1073, issn 0022-3042, 10 p.Article

A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseNISHIOKA, Kenya; KEFI, Mounir; AMOURI, Rim et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 4, pp 391-395, issn 0022-3050, 5 p.Article

Familial Association of Inflammatory Bowel Diseases With Other Autoimmune and Related DiseasesHEMMINKI, Kari; XINJUN LI; SUNDQUIST, Kristina et al.The American journal of gastroenterology. 2010, Vol 105, Num 1, pp 139-147, issn 0002-9270, 9 p.Article

Familial Micronodular Adrenocortical Disease, Cushing Syndrome, and Mutations of the Gene Encoding Phosphodiesterase 11 A4 (PDE11A)CARNEY, J. Aidan; GAILLARD, Rolf C; BERTHERAT, Jérôme et al.The American journal of surgical pathology. 2010, Vol 34, Num 4, pp 547-555, issn 0147-5185, 9 p.Article

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial diseaseWOODS, M. O; YOUNGHUSBAND, H. B; DE LA CHAPELLE, A et al.Gut. 2010, Vol 59, Num 10, pp 1369-1377, issn 0017-5749, 9 p.Article

Hippocampal Hyperactivation in Presymptomatic Familial Alzheimer's DiseaseQUIROZ, Yakeel T; BUDSON, Andrew E; CELONE, Kim et al.Annals of neurology. 2010, Vol 68, Num 6, pp 865-875, issn 0364-5134, 11 p.Article

Age-Related Vascular Pathology in Transgenic Mice Expressing Presenilin 1-Associated Familial Alzheimer's Disease MutationsGAMA SOSA, Miguel A; DE GASPERI, Rita; ELDER, Gregory A et al.The American journal of pathology. 2010, Vol 176, Num 1, pp 353-368, issn 0002-9440, 16 p.Article

Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: An independent pathogenic roleCHAODONG WANG; HUILI MA; XIULI FENG et al.Brain research. 2010, Vol 1358, pp 30-38, issn 0006-8993, 9 p.Article

Familial Ménière's disease: clinical and genetic aspectsMORRISON, A. W; BAILEY, M. E. S; MORRISON, G. A. J et al.Journal of laryngology and otology. 2009, Vol 123, Num 1, pp 29-37, issn 0022-2151, 9 p.Article

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onsetNICHOLS, W. C; PANKRATZ, N; MAREK, D. K et al.Neurology. 2009, Vol 72, Num 4, pp 310-316, issn 0028-3878, 7 p.Article

Differences in characteristics and risk of cardiovascular disease in familial hypercholesterolemia patients with and without tendon xanthomas: A systematic review and meta-analysisOOSTERVEER, Daniëlla M; VERSMISSEN, Jorie; YAZDANPANAH, Mojgan et al.Atherosclerosis. 2009, Vol 207, Num 2, pp 311-317, issn 0021-9150, 7 p.Article