Detalhe da pesquisa
1.
Feasibility of developing a pediatric telehealth network in Honduras with international consultation support.
Rural Remote Health
; 17(2): 3965, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28564548
2.
A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features.
Am J Med Genet A
; 170(12): 3313-3318, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27570168
3.
Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.
Am J Med Genet A
; 164A(11): 2887-91, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25123844
4.
ß-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation.
Brain
; 136(Pt 6): 1708-17, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23687123
5.
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
Am J Hum Genet
; 83(2): 170-9, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18674751
6.
Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature.
Am J Med Genet A
; 155A(9): 2146-53, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21834054
7.
Reduction in rate of epilepsy from neurocysticercosis by community interventions: the Salamá, Honduras study.
Epilepsia
; 52(6): 1177-85, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21275975
8.
Autism in two females with duplications involving Xp11.22-p11.23.
Dev Med Child Neurol
; 53(5): 463-6, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21418194
9.
United States head circumference growth reference charts: birth to 21 years.
J Pediatr
; 156(6): 907-913.e2, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20304425
10.
Natural history of Christianson syndrome.
Am J Med Genet A
; 152A(11): 2775-83, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20949524
11.
Pediatric convulsive status epilepticus in Honduras, Central America.
Epilepsia
; 50(10): 2314-9, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19694798
12.
Adherence and complementary and alternative medicine use among Honduran people with epilepsy.
Epilepsy Behav
; 14(4): 645-50, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19435580
13.
Heads you win, tails you lose: measuring head circumference.
Dev Med Child Neurol
; 56(8): 705, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24660758
14.
ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration.
J Clin Invest
; 129(5): 2145-2162, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30985297
15.
Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
J Child Neurol
; 23(1): 112-7, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18184946
16.
Developing a neurology training program in Honduras: a joint project of neurologists in Honduras and the World Federation of Neurology.
J Neurol Sci
; 253(1-2): 7-17, 2007 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17188302
17.
Expansion of the deletion 13q syndrome phenotype: a case report.
J Child Neurol
; 22(9): 1124-7, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17890413
18.
Clinical Features and Neurologic Complications of Children Hospitalized With Chikungunya Virus in Honduras.
J Child Neurol
; 32(8): 712-716, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28459170
19.
Transgenerational Inheritance of Familial Lipomyelomeningocele.
J Child Neurol
; 32(14): 1118-1122, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29129155
20.
Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts.
Neuromuscul Disord
; 16(2): 132-6, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16427280