Brancati F - Search Results

1

Primary hypothyroidism and osteopenia associated with Neuhauser syndrome.

Sarkozy A, Mingarelli R, Brancati F, Dallapiccola B. Sarkozy A, et al. Among authors: brancati f. Am J Med Genet. 2002 Sep 1;111(4):412-4. doi: 10.1002/ajmg.10577. Am J Med Genet. 2002. PMID: 12210302

2

Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women.

Semprini S, Mango R, Brancati F, Dallapiccola B, Becherini L, Novelli G, De Lorenzo A, Brandi ML, Gennari L. Semprini S, et al. Among authors: brancati f. Calcif Tissue Int. 2000 Jul;67(1):93-4. doi: 10.1007/s00223001103. Calcif Tissue Int. 2000. PMID: 10908420

3

A single strand conformation polymorphism-based carrier test for spinal muscular atrophy.

Semprini S, Tacconelli A, Capon F, Brancati F, Dallapiccola B, Novelli G. Semprini S, et al. Among authors: brancati f. Genet Test. 2001 Spring;5(1):33-7. doi: 10.1089/109065701750168662. Genet Test. 2001. PMID: 11336398

4

PARK6-linked parkinsonism occurs in several European families.

Valente EM, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Wassilowsky D, Harhangi BS, Rawal N, Caputo V, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease. Valente EM, et al. Among authors: brancati f. Ann Neurol. 2002 Jan;51(1):14-8. Ann Neurol. 2002. PMID: 11782979

5

Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia.

Brancati F, Defazio G, Caputo V, Valente EM, Pizzuti A, Livrea P, Berardelli A, Dallapiccola B. Brancati F, et al. Mov Disord. 2002 Mar;17(2):392-7. doi: 10.1002/mds.10077. Mov Disord. 2002. PMID: 11921130

6

Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34.

Valente EM, Brancati F, Caputo V, Bertini E, Patrono C, Costanti D, Dallapiccola B. Valente EM, et al. Among authors: brancati f. Ann Neurol. 2002 Jun;51(6):681-5. doi: 10.1002/ana.10204. Ann Neurol. 2002. PMID: 12112072

7

Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.

Defazio G, Brancati F, Valente EM, Caputo V, Pizzuti A, Martino D, Abbruzzese G, Livrea P, Berardelli A, Dallapiccola B. Defazio G, et al. Among authors: brancati f. Mov Disord. 2003 Feb;18(2):207-12. doi: 10.1002/mds.10314. Mov Disord. 2003. PMID: 12539217

8

PARK6 is a common cause of familial parkinsonism.

Valente EM, Brancati F, Caputo V, Graham EA, Davis MB, Ferraris A, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease. Valente EM, et al. Among authors: brancati f. Neurol Sci. 2002 Sep;23 Suppl 2:S117-8. doi: 10.1007/s100720200097. Neurol Sci. 2002. PMID: 12548371

9

Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia.

Brancati F, Valente EM, Castori M, Vanacore N, Sessa M, Galardi G, Berardelli A, Bentivoglio AR, Defazio G, Girlanda P, Abbruzzese G, Albanese A, Dallapiccola B; Italian Movement Disorder Study Group. Brancati F, et al. J Neurol Neurosurg Psychiatry. 2003 May;74(5):665-6. doi: 10.1136/jnnp.74.5.665. J Neurol Neurosurg Psychiatry. 2003. PMID: 12700316 Free PMC article.

10

Description, nomenclature, and mapping of a novel cerebello-renal syndrome with the molar tooth malformation.

Valente EM, Salpietro DC, Brancati F, Bertini E, Galluccio T, Tortorella G, Briuglia S, Dallapiccola B. Valente EM, et al. Among authors: brancati f. Am J Hum Genet. 2003 Sep;73(3):663-70. doi: 10.1086/378241. Epub 2003 Aug 7. Am J Hum Genet. 2003. PMID: 12908130 Free PMC article.

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