Arena F - Search Results

1

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D, et al. Tranebjaerg L, et al. Among authors: arena f. J Med Genet. 1995 Apr;32(4):257-63. doi: 10.1136/jmg.32.4.257. J Med Genet. 1995. PMID: 7643352 Free PMC article.

2

MRX8: an X-linked mental retardation condition with linkage to Xq21.

Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE. Schwartz CE, et al. Among authors: arena f. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):467-74. doi: 10.1002/ajmg.1320430170. Am J Med Genet. 1992. PMID: 1605227

3

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness.

Jin H, May M, Tranebjaerg L, Kendall E, Fontán G, Jackson J, Subramony SH, Arena F, Lubs H, Smith S, Stevenson R, Schwartz C, Vetrie D. Jin H, et al. Among authors: arena f. Nat Genet. 1996 Oct;14(2):177-80. doi: 10.1038/ng1096-177. Nat Genet. 1996. PMID: 8841189

4

X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.

Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE. Armfield K, et al. Among authors: arena f. Am J Med Genet. 1999 Jul 30;85(3):236-42. doi: 10.1002/(sici)1096-8628(19990730)85:3<236::aid-ajmg10>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10398235

5

XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28.

Lubs H, Abidi F, Bier JA, Abuelo D, Ouzts L, Voeller K, Fennell E, Stevenson RE, Schwartz CE, Arena F. Lubs H, et al. Among authors: arena f. Am J Med Genet. 1999 Jul 30;85(3):243-8. doi: 10.1002/(sici)1096-8628(19990730)85:3<243::aid-ajmg11>3.0.co;2-e. Am J Med Genet. 1999. PMID: 10398236

6

XLMR genes: update 1992.

Neri G, Chiurazzi P, Arena F, Lubs HA, Glass IA. Neri G, et al. Among authors: arena f. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):373-82. doi: 10.1002/ajmg.1320430158. Am J Med Genet. 1992. PMID: 1605215 Review.

7

Evidence for a BRCA1 founder mutation in families of West African ancestry.

Mefford HC, Baumbach L, Panguluri RC, Whitfield-Broome C, Szabo C, Smith S, King MC, Dunston G, Stoppa-Lyonnet D, Arena F. Mefford HC, et al. Among authors: arena f. Am J Hum Genet. 1999 Aug;65(2):575-8. doi: 10.1086/302511. Am J Hum Genet. 1999. PMID: 10417303 Free PMC article. No abstract available.

8

Research on heterocyclic compounds. XXX. Synthesis and pharmacological activity of 2-methylimidazo[1,2-b]pyridazine-3-carboxylic acids.

Abignente E, Arena F, Luraschi E, Saturnino C, Rossi F, Berrino L, Cenicola ML. Abignente E, et al. Among authors: arena f. Farmaco. 1992 Jun;47(6):931-44. Farmaco. 1992. PMID: 1388610

9

Research on heterocyclic compounds. XXVI. Antiinflammatory and related activities of some 2-phenylimidazo[1,2-b]pyridazines.

Abignente E, Arena F, Luraschi E, De Caprariss P, Marmo E, Vitagliano S, Donnoli D. Abignente E, et al. Among authors: arena f. Res Commun Chem Pathol Pharmacol. 1990 Jan;67(1):43-54. Res Commun Chem Pathol Pharmacol. 1990. PMID: 2326548

10

Research on heterocyclic compounds. XXII. Imidazo[1,2-a]pyrimidines.

Abignente E, Arena F, Luraschi E, Saturnino C, Berrino L, De Santis D, Marmo E. Abignente E, et al. Among authors: arena f. Farmaco Sci. 1987 Sep;42(9):657-69. Farmaco Sci. 1987. PMID: 3500872

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