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1.
Prevalence and Clinical Factors Associated With Pes Planus Among Children and Adults: A Population-Based Synthesis and Systematic Review.
J Foot Ankle Surg
; 62(5): 899-903, 2023.
Article
in English
| MEDLINE | ID: mdl-37286098
2.
Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall.
Int J Mol Sci
; 20(9)2019 May 09.
Article
in English
| MEDLINE | ID: mdl-31075877
3.
Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution.
Pediatr Surg Int
; 34(3): 277-282, 2018 Mar.
Article
in English
| MEDLINE | ID: mdl-29335896
4.
Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?
Pediatr Surg Int
; 34(5): 505-514, 2018 May.
Article
in English
| MEDLINE | ID: mdl-29550988
5.
A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis.
Pediatr Surg Int
; 34(9): 931-943, 2018 Sep.
Article
in English
| MEDLINE | ID: mdl-30094464
6.
Say-Meyer syndrome: additional manifestations in a new patient and phenotypic assessment.
Childs Nerv Syst
; 31(7): 1181-7, 2015 Jul.
Article
in English
| MEDLINE | ID: mdl-25904354
7.
Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis.
Mol Genet Genomic Med
; 8(5): e1176, 2020 05.
Article
in English
| MEDLINE | ID: mdl-32163230
8.
Genetic Variants at the rs4720169 Locus of TBX20 and the rs12921862 Locus of AXIN1 May Increase the Risk of Congenital Heart Defects in the Mexican Population: A Pilot Study.
Genet Test Mol Biomarkers
; 23(9): 664-670, 2019 Sep.
Article
in English
| MEDLINE | ID: mdl-31524541
9.
Evaluation of familial factors in a Mexican population-based setting with gastroschisis: Further evidence for an underlying genetic susceptibility.
J Pediatr Surg
; 53(3): 521-524, 2018 Mar.
Article
in English
| MEDLINE | ID: mdl-28935396
10.
Prevalence, Mortality, and Spatial Distribution of Gastroschisis in Mexico.
J Pediatr Adolesc Gynecol
; 31(3): 232-237, 2018 Jun.
Article
in English
| MEDLINE | ID: mdl-29317257
11.
Severe Intrauterine Amputations in One Dichorionic Twin With Pentalogy of Cantrell: Further Evidence and Consideration for Mechanical Teratogenesis.
Pediatr Dev Pathol
; 20(5): 440-443, 2017.
Article
in English
| MEDLINE | ID: mdl-28812462
12.
Fetus with Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of a Novel Association and Review of the Phenotype.
Pediatr Dev Pathol
; 19(2): 159-64, 2016.
Article
in English
| MEDLINE | ID: mdl-26367183
13.
Otofaciocervical syndrome and metachondromatosis in a girl: Presentation of a novel association and remarks on clinical variability of branchial-arch disorders.
Int J Pediatr Otorhinolaryngol
; 85: 19-21, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-27240490
14.
Clinical, cytogenetic, environmental and inheritance findings in Mexican neonates with VACTERL association.
Indian J Pediatr
; 82(1): 84-8, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25008186
15.
[Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome]. / Anomalías inusuales del arco branquial, dermoepidérmicas y del sistema nervioso en un neonato con el síndrome VACTERL-H.
Arch Argent Pediatr
; 110(4): e67-71, 2012 Aug.
Article
in Spanish
| MEDLINE | ID: mdl-22859335
16.
Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient.
Acta Neurol Belg
; 116(2): 229-31, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-26194037
17.
Branchiootorenal syndrome with skeletal defects: a novel association in a Mexican child.
Clin Dysmorphol
; 24(1): 21-3, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25380322
18.
Male-to-male transmission of Laurin-Sandrow syndrome in a Mexican family.
Clin Dysmorphol
; 23(2): 39-41, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-24556604
19.
Anomalías inusuales del arco branquial, dermoepidérmicas y del sistema nervioso en un neonato con el síndrome VACTERL-H / Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome
Arch. argent. pediatr
; 110(4): e67-e71, ago. 2012. ilus, tab
Article
in Spanish
| LILACS | ID: lil-657467
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