Ajmar F - Search Results

1

Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study.

Di Maria E, Gulli R, Begni S, De Luca A, Bignotti S, Pasini A, Bellone E, Pizzuti A, Dallapiccola B, Novelli G, Ajmar F, Gennarelli M, Mandich P. Di Maria E, et al. Among authors: ajmar f. Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):27-9. doi: 10.1002/ajmg.b.30028. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15211626

2

Essential tremor is not associated with alpha-synuclein gene haplotypes.

Pigullo S, Di Maria E, Marchese R, Bellone E, Gulli R, Scaglione C, Battaglia S, Barone P, Martinelli P, Abbruzzese G, Ajmar F, Mandich P. Pigullo S, et al. Among authors: ajmar f. Mov Disord. 2003 Jul;18(7):823-6. doi: 10.1002/mds.10421. Mov Disord. 2003. PMID: 12815663

3

mRNA distribution in adult human brain of GRIN2B, a N-methyl-D-aspartate (NMDA) receptor subunit.

Schito AM, Pizzuti A, Di Maria E, Schenone A, Ratti A, Defferrari R, Bellone E, Mancardi GL, Ajmar F, Mandich P. Schito AM, et al. Among authors: ajmar f. Neurosci Lett. 1997 Dec 12;239(1):49-53. doi: 10.1016/s0304-3940(97)00853-7. Neurosci Lett. 1997. PMID: 9547169

4

Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremor.

Pigullo S, De Luca A, Barone P, Marchese R, Bellone E, Colosimo A, Scaglione C, Martinelli P, Di Maria E, Pizzuti A, Abbruzzese G, Dallapiccola B, Ajmar F, Mandich P. Pigullo S, et al. Among authors: ajmar f. Parkinsonism Relat Disord. 2004 Aug;10(6):357-62. doi: 10.1016/j.parkreldis.2004.04.012. Parkinsonism Relat Disord. 2004. PMID: 15261877

5

Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12.

Mandich P, Schito AM, Bellone E, Antonacci R, Finelli P, Rocchi M, Ajmar F. Mandich P, et al. Among authors: ajmar f. Genomics. 1994 Jul 1;22(1):216-8. doi: 10.1006/geno.1994.1366. Genomics. 1994. PMID: 7959773

6

Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II.

Mandich P, Bellone E, Di Maria E, Pigullo S, Pizzuti A, Schenone A, Soriani S, Varese A, Windebank AJ, Ajmar F. Mandich P, et al. Among authors: ajmar f. Am J Med Genet. 1999 Apr 23;83(5):409-10. Am J Med Genet. 1999. PMID: 10232753

7

Mental function in males and females.

Ajmar F, Di Maria E, Padovani L. Ajmar F, et al. Am J Med Genet. 1999 Dec 15;88(6):593. doi: 10.1002/(sici)1096-8628(19991215)88:6<593::aid-ajmg1>3.0.co;2-j. Am J Med Genet. 1999. PMID: 10581472 No abstract available.

8

A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect.

Di Maria E, Gulli R, Balestra P, Cassandrini D, Pigullo S, Doria-Lamba L, Bado M, Schenone A, Ajmar F, Mandich P, Bellone E. Di Maria E, et al. Among authors: ajmar f. J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1495-8. doi: 10.1136/jnnp.2003.028100. J Neurol Neurosurg Psychiatry. 2004. PMID: 15377708 Free PMC article.

9

Genetic analysis of Huntington disease in Italy.

Ajmar F, Mandich P, Bellone E, Abbruzzese G. Ajmar F, et al. Am J Med Genet. 1991 May 1;39(2):211-4. doi: 10.1002/ajmg.1320390219. Am J Med Genet. 1991. PMID: 1829583

10

Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney Disease.

Mandich P, Restagno G, Novelli G, Bellone E, Potenza L, Varetto O, Dallapiccola B, Carbonara A, Ajmar F. Mandich P, et al. Among authors: ajmar f. Am J Med Genet. 1990 Apr;35(4):579-81. doi: 10.1002/ajmg.1320350426. Am J Med Genet. 1990. PMID: 2333889

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