Carrizosa J - Search Results

1

A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset.

Pineda-Trujillo N, Cornejo W, Carrizosa J, Wheeler RB, Múnera S, Valencia A, Agudelo-Arango J, Cogollo A, Anderson G, Bedoya G, Mole SE, Ruíz-Linares A. Pineda-Trujillo N, et al. Among authors: carrizosa j. Neurology. 2005 Feb 22;64(4):740-2. doi: 10.1212/01.WNL.0000151974.44980.F1. Neurology. 2005. PMID: 15728307

2

A novel SCN1A mutation associated with severe GEFS+ in a large South American pedigree.

Pineda-Trujillo N, Carrizosa J, Cornejo W, Arias W, Franco C, Cabrera D, Bedoya G, Ruíz-Linares A. Pineda-Trujillo N, et al. Among authors: carrizosa j. Seizure. 2005 Mar;14(2):123-8. doi: 10.1016/j.seizure.2004.12.007. Seizure. 2005. PMID: 15694566 Free article.

3

[Genetic linkage analysis of Gilles de la Tourette Syndrome in a Colombian family].

García-Cerén JJ, Valencia-Duarte AV, Cornejo JW, Carrizosa J, Cuartas JM, Zuluaga-Espinosa NA, Bedoya G, Ruiz-Linares A. García-Cerén JJ, et al. Among authors: carrizosa j. Rev Neurol. 2006 Feb 16-28;42(4):211-6. Rev Neurol. 2006. PMID: 16521059 Free article. Spanish.

4

[Clinical characteristics of optical neuritis in children].

Franco AF, Cabrera D, Carrizosa J, Cornejo W. Franco AF, et al. Among authors: carrizosa j. Rev Neurol. 2003 Feb 1-15;36(3):208-11. Rev Neurol. 2003. PMID: 12599148 Free article. Spanish.

5

[Cerebrovascular disease in children with sickle cell anaemia].

Carrizosa J, Lopera JE, Cornejo W. Carrizosa J, et al. Rev Neurol. 2003 Sep 16-30;37(6):511-4. Rev Neurol. 2003. PMID: 14533066 Free article. Spanish.

6

[Clinical characterisation and power simulations to detect genetic linkage in attention deficit hyperactivity disorder in Antioquian families].

Cornejo W, Cuartas M, Gómez-Uribe LF, Carrizosa J, Rivas I, Castillo H, Bedoya G, Ruiz A. Cornejo W, et al. Among authors: carrizosa j. Rev Neurol. 2004 Feb 16-29;38(4):319-22. Rev Neurol. 2004. PMID: 14997454 Free article. Spanish.

7

[Evidence for association and epistasis between the genetic markers SLC6A4 and HTR2A in autism etiology].

Valencia AV, Páez AL, Sampedro ME, Ávila C, Cardona JC, Mesa C, Galvis L, Carrizosa J, Camargo M, Ruiz A, Cornejo W, Bedoya G. Valencia AV, et al. Among authors: carrizosa j. Biomedica. 2012 Oct-Dec;32(4):585-601. doi: 10.1590/S0120-41572012000400014. Biomedica. 2012. PMID: 23715234 Spanish.

8

[Clinical and radiological findings in two cases of aspergillosis of the central nervous system in children].

Blazicevich-Carrillo L, Cabrales- Camacho LM, Carrizosa J, Cornejo W. Blazicevich-Carrillo L, et al. Among authors: carrizosa j. Rev Neurol. 2003 Apr 1-15;36(7):632-5. Rev Neurol. 2003. PMID: 12666043 Free article. Spanish.

9

Segregation of a haplotype encompassing FEB1 with genetic epilepsy with febrile seizures plus in a Colombian family.

Caro-Gomez MA, Carrizosa J, Moreno JT, Cabrera D, Bedoya G, Ruiz-Linares A, Franco A, Gomez-Castillo C, Cornejo W, Pineda-Trujillo N. Caro-Gomez MA, et al. Among authors: carrizosa j. Epileptic Disord. 2013 Jun;15(2):128-31. doi: 10.1684/epd.2013.0570. Epileptic Disord. 2013. PMID: 23773973 Free article.

10

[Prevalence of attention deficit hyperactivity disorder in Colombian children and teenagers].

Cornejo JW, Osío O, Sánchez Y, Carrizosa J, Sánchez G, Grisales H, Castillo-Parra H, Holguín J. Cornejo JW, et al. Among authors: carrizosa j. Rev Neurol. 2005 Jun 16-30;40(12):716-22. Rev Neurol. 2005. PMID: 15973636 Free article. Spanish.

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