Cobo AM - Search Results

1

A neonatal form of Steinert's myotonic dystrophy in twins after in vitro fertilization.

García de Andoin N, Echeverría J, Cobo AM, Rey A, Paisán L, López de Munain A. García de Andoin N, et al. Among authors: cobo am. Fertil Steril. 2005 Sep;84(3):756. doi: 10.1016/j.fertnstert.2005.03.062. Fertil Steril. 2005. PMID: 16169416 Free article.

2

Influence of the sex of the transmitting grandparent in congenital myotonic dystrophy.

López de Munain A, Cobo AM, Poza JJ, Navarrete D, Martorell L, Palau F, Emparanza JI, Baiget M. López de Munain A, et al. Among authors: cobo am. J Med Genet. 1995 Sep;32(9):689-91. doi: 10.1136/jmg.32.9.689. J Med Genet. 1995. PMID: 8544186 Free PMC article.

3

Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy.

López de Munain A, Cobo AM, Sáenz A, Blanco A, Poza JJ, Martorell L, Martí-Massó JF, Baiget M. López de Munain A, et al. Among authors: cobo am. Genet Epidemiol. 1996;13(5):483-7. doi: 10.1002/(SICI)1098-2272(1996)13:5<483::AID-GEPI4>3.0.CO;2-3. Genet Epidemiol. 1996. PMID: 8905394

4

Anticipation in myotonic dystrophy: a parental-sex-related phenomenon.

López de Munain A, Blanco A, Emparanza JI, Martí Massó JF, Cobo A, Basauri B, Martorell L, Baiget M, Martínez Lage JM. López de Munain A, et al. Neuroepidemiology. 1994;13(1-2):75-8. doi: 10.1159/000110362. Neuroepidemiology. 1994. PMID: 8190210

5

Prevalence of myotonic dystrophy in Guipúzcoa (Basque Country, Spain).

López de Munain A, Blanco A, Emparanza JI, Poza JJ, Martí Massó JF, Cobo A, Martorell L, Baiget M, Martínez Lage JM. López de Munain A, et al. Neurology. 1993 Aug;43(8):1573-6. doi: 10.1212/wnl.43.8.1573. Neurology. 1993. PMID: 8351014

6

Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophy.

Cobo AM, Poza JJ, Martorell L, López de Munain A, Emparanza JI, Baiget M. Cobo AM, et al. J Med Genet. 1995 Feb;32(2):105-8. doi: 10.1136/jmg.32.2.105. J Med Genet. 1995. PMID: 7760317 Free PMC article.

7

Frequency of myotonic dystrophy gene carriers in cataract patients.

Cobo AM, Poza JJ, Blanco A, López de Munain A, Saénz A, Azpitarte M, Marchessi J, Martí Massó JF. Cobo AM, et al. J Med Genet. 1996 Mar;33(3):221-3. doi: 10.1136/jmg.33.3.221. J Med Genet. 1996. PMID: 8728695 Free PMC article.

8

Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1.

Sistiaga A, Urreta I, Jodar M, Cobo AM, Emparanza J, Otaegui D, Poza JJ, Merino JJ, Imaz H, Martí-Massó JF, López de Munain A. Sistiaga A, et al. Among authors: cobo am. Psychol Med. 2010 Mar;40(3):487-95. doi: 10.1017/S0033291709990602. Epub 2009 Jul 23. Psychol Med. 2010. PMID: 19627641

9

[Application of the polymerase chain reaction technique (PCR) to the molecular diagnosis of myotonic dystrophy].

Cobo AM, Martínez JM, López de Munain A, Baiget M. Cobo AM, et al. Neurologia. 1991 Nov;6(9):317-21. Neurologia. 1991. PMID: 1687310 Spanish.

10

[Basic concepts in molecular genetics].

Cobo AM, Poza JJ, Sáenz A, López de Munain A. Cobo AM, et al. Rev Neurol. 1996 Mar;24(127):315-9. Rev Neurol. 1996. PMID: 8742399 Review. Spanish. No abstract available.

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