Figuera LE - Search Results

1

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.

Dávalos NO, García-Vargas A, Pforr J, Dávalos IP, Picos-Cárdenas VJ, García-Cruz D, Kruse R, Figuera LE, Nöthen MM, Betz RC. Dávalos NO, et al. Among authors: figuera le. Br J Dermatol. 2005 Dec;153(6):1216-9. doi: 10.1111/j.1365-2133.2005.06958.x. Br J Dermatol. 2005. PMID: 16307662

2

SOD1 gene variants rs4817415, rs2070424, and rs1041740 and their association with breast cancer risk.

Gallegos-Arreola MP, Márquez-Rosales MG, Gómez-Meda BC, Zúñiga-González GM, Puebla-Pérez AM, Zamora-Pérez AL, Delgado-Saucedo JI, Figuera LE. Gallegos-Arreola MP, et al. Among authors: figuera le. Eur Rev Med Pharmacol Sci. 2023 Apr;27(7):3088-3095. doi: 10.26355/eurrev_202304_31943. Eur Rev Med Pharmacol Sci. 2023. PMID: 37070912 Free article.

3

Guadalajara camptodactyly syndrome type I. A corroborative family.

Figuera LE, Ramírez-Dueñas ML, García-Cruz D, Villar V, Cantú JM. Figuera LE, et al. Clin Genet. 1993 Jan;43(1):11-5. doi: 10.1111/j.1399-0004.1993.tb04418.x. Clin Genet. 1993. PMID: 7681735

4

The Myhre syndrome: report of two cases.

García-Cruz D, Figuera LE, Feria-Velazco A, Sánchez-Corona J, García-Cruz MO, Ramírez-Duenãs RM, Hernandez-Córdova A, Ruiz MX, Bitar-Alatorre WE, Ramírez-Dueñas ML, et al. García-Cruz D, et al. Among authors: figuera le. Clin Genet. 1993 Oct;44(4):203-7. doi: 10.1111/j.1399-0004.1993.tb03880.x. Clin Genet. 1993. PMID: 8261650

5

Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation.

Figuera LE, García-Cruz D, Ramírez-Dueñas ML, Rivera-Robles V, Cantù JM. Figuera LE, et al. Clin Genet. 1993 Aug;44(2):98-101. doi: 10.1111/j.1399-0004.1993.tb03855.x. Clin Genet. 1993. PMID: 8275567

6

Molecular characterization of the fragile-X syndrome in the Mexican population.

Díaz-Gallardo MY, Barros-Núñez P, Díaz CA, Hernández A, Gómez-Espinel I, Leal CA, Fragoso R, Figuera L, García-Cruz D, Ramírez-Dueñas ML. Díaz-Gallardo MY, et al. Arch Med Res. 1995;26 Spec No:S77-83. Arch Med Res. 1995. PMID: 8845662

7

Floating-Harbor syndrome. A neuropsychological approach.

Davalos IP, Figuera LE, Bobadilla L, Martinez-Martinez R, Matute E, Partida MG, Bañuelos LA, Ramirez-Dueñas ML. Davalos IP, et al. Among authors: figuera le. Genet Couns. 1996;7(4):283-8. Genet Couns. 1996. PMID: 8985732

8

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome.

Garcia-Cruz D, Sánchez-Corona J, Nazará Z, Garcia-Crúz MO, Figuera LE, Castañeda V, Cantú JM. Garcia-Cruz D, et al. Among authors: figuera le. Am J Med Genet. 1997 Mar 17;69(2):138-51. doi: 10.1002/(sici)1096-8628(19970317)69:2<138::aid-ajmg5>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9056550

9

Inherited hypertrichoses.

Garcia-Cruz D, Figuera LE, Cantu JM. Garcia-Cruz D, et al. Among authors: figuera le. Clin Genet. 2002 May;61(5):321-9. doi: 10.1034/j.1399-0004.2002.610501.x. Clin Genet. 2002. PMID: 12081714 Review.

10

Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome.

Figuera LE, Ramírez-Dueñas ML, Dávalos IP, Cantú JM. Figuera LE, et al. Clin Dysmorphol. 2002 Oct;11(4):243-7. doi: 10.1097/00019605-200210000-00003. Clin Dysmorphol. 2002. PMID: 12401988

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