Caractérisation moléculaire de SMARCB1 et NF2 dans la schwannomatose familiale et sporadique : un paradigme qui évolue = Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis : An evolving paradigmDEREURE, O.Annales de dermatologie et de vénéréologie. 2009, Vol 136, Num 3, pp 296-297, issn 0151-9638, 2 p.Article

Pachyleuconychie longitudinale, forme sporadique ? = Longitudinal pachyleukonychia, a sporadic form?WAGSCHAL, Daniel.Les Nouvelles dermatologiques. 2011, Vol 30, Num JUN, pp 311-312, issn 0752-5370, 2 p., CAH1Article

A genome-wide association study of sporadic ALS in a homogenous Irish populationCRONIN, Simon; BERGER, Stephen; JINHUI DING et al.Human molecular genetics (Print). 2008, Vol 17, Num 5, pp 768-774, issn 0964-6906, 7 p.Article

Mutations in VAPB are not associated with sporadic ALSKIRBY, J; HEWAMADDUMA, C. A. A; HARTLEY, J. A et al.Neurology. 2007, Vol 68, Num 22, pp 1951-1953, issn 0028-3878, 3 p.Article

When sporadic disease is not sporadic: The potential for genetic etiologyGOLDMAN, Jill S; MILLER, Bruce L; SAFAR, Jiri et al.Archives of neurology (Chicago). 2004, Vol 61, Num 2, pp 213-216, issn 0003-9942, 4 p.Article

No CCM2 mutations in a cohort of 31 sporadic casesVERLAAN, D. J; LAURENT, S. B; ROULEAU, G. A et al.Neurology. 2004, Vol 63, Num 10, issn 0028-3878, p. 1979Article

Clinical characteristics and surgical treatment of sporadic primary hyperparathyroidism with emphasis on chief cell hyperplasiaWALLFELT, C; LJUNGHALL, S; BERGSTROM, R et al.Surgery. 1990, Vol 107, Num 1, pp 13-19, issn 0039-6060Article

LACK OF ASSOCIATION BETWEEN VEGF GENE POLYMORPHISMS AND PLASMA VEGF LEVELS AND SPORADIC ALSGOLENIA, A; TOMIK, B; ZAWISLAK, D et al.Neurology. 2010, Vol 75, Num 22, pp 2035-2037, issn 0028-3878, 3 p.Article

A novel nonsense mutation in PAX9 is associated with sporadic hypodontiaJUNXIA ZHU; XIANG YANG; CHENYING ZHANG et al.Mutagenesis. 2012, Vol 27, Num 3, pp 313-317, issn 0267-8357, 5 p.Article

Caractérisation moléculaire de SMARCB1 et NF2 dans la schwannomatose familiale et sporadique : un paradigme qui évolue = Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis : An evolving paradigmDEREURE, O.Annales de dermatologie et de vénéréologie. 2008, Vol 135, Num 12, pp 888-889, issn 0151-9638, 2 p.Article

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2HOULDEN, H; LAURA, M; WAVRANT-DE VRIEZE, F et al.Neurology. 2008, Vol 71, Num 21, pp 1660-1668, issn 0028-3878, 9 p.Article

Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosisHADFIELD, K. D; NEWMAN, W. G; BOWERS, N. L et al.Journal of medical genetics. 2008, Vol 45, Num 6, pp 332-339, issn 0022-2593, 8 p.Article

Sequence analysis of tau 3'untranslated region and saitohin gene in sporadic progressive supranuclear palsyEZQUERRA, M; CAMPDELACREU, J; MUNOZ, E et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 1, pp 155-157, issn 0022-3050, 3 p.Article

SMN1 gene duplications are associated with sporadic ALSBLAUW, H. M; BARNES, C. P; VAN VUGHT, P. W. J et al.Neurology. 2012, Vol 78, Num 11, pp 776-780, issn 0028-3878, 5 p.Article

Hipertricosis cervical anterior esporádica. Respuesta de los autores = Sporadic Anterior Cervical Hypertrichosis. Authors' replyMORENO-GIMENEZ, J. C; CAMACHO-MARTINEZ, F. M; MONTEAGUDO, B et al.Actas dermo-sifiliográficas (Ed. impresa). 2009, Vol 100, Num 9, pp 833-836, issn 0001-7310, 4 p.Article

SMN1 gene, but not SMN2, is a risk factor for sporadic ALSCORCIA, P; CAMU, W; HALIMI, J.-M et al.Neurology. 2006, Vol 67, Num 7, pp 1147-1150, issn 0028-3878, 4 p.Article

The cognitive profiles of CADASIL and sporadic small vessel diseaseCHARLTON, R. A; MORRIS, R. G; NITKUNAN, A et al.Neurology. 2006, Vol 66, Num 10, pp 1523-1526, issn 0028-3878, 4 p.Article

No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALSBROOM, W. J; PARTON, M. J; VANCE, C. A et al.Neurology. 2004, Vol 63, Num 12, pp 2419-2422, issn 0028-3878, 4 p.Article

Distribution function of the sporadic E-layer screening frequencyLUKIN, A. N; MOISEEV, S. N.Radiophysics and quantum electronics. 1991, Vol 34, Num 8, pp 705-709, issn 0033-8443Article

Absorption anormale des ondes radioélectriques tests dans une couche sporadique d'ionosphère EBOJKO, G. N; ZYUZIN, V. A; METELEV, S. A et al.Izvestiâ vysših učebnyh zavedenij. Radiofizika. 1987, Vol 30, Num 5, pp 671-673, issn 0021-3462Article

Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBMCHAHIN, Nizar; ENGEL, Andrew G.Neurology. 2008, Vol 70, Num 6, pp 418-424, issn 0028-3878, 7 p.Article

Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALSBLAIN, C. R. V; BRUNTON, S; WILLIAMS, S. C. R et al.Journal of neurology, neurosurgery and psychiatry. 2011, Vol 82, Num 8, pp 843-849, issn 0022-3050, 7 p.Article

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaBRUSSINO, A; GELLERA, C; MIGONE, N et al.Neurology. 2005, Vol 64, Num 1, pp 145-147, issn 0028-3878, 3 p.Article

No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutationsSCHWARTZ, Marianne; VISSING, John.Journal of the neurological sciences. 2004, Vol 218, Num 1-2, pp 99-101, issn 0022-510X, 3 p.Article

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusionsCAIRNS, Nigel J; NEUMANN, Manuela; CARTER, Deborah et al.The American journal of pathology. 2007, Vol 171, Num 1, pp 227-240, issn 0002-9440, 14 p.Article