Detalhe da pesquisa
1.
Diagnosis and Treatment of Lacrimal Gland Prolapse: A Narrative Review.
Aesthetic Plast Surg
; 2024 May 13.
Artigo
Inglês
| MEDLINE | ID: mdl-38740621
2.
Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder.
Genet Med
; 25(9): 100893, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37179472
3.
Dietary Antioxidant Capacity Indices are Negatively Correlated to LDL-Oxidation in Adults.
Int J Clin Pract
; 2023: 5446163, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36950308
4.
Tissue Extract from Brittle Star Undergoing Arm Regeneration Promotes Wound Healing in Rat.
Mar Drugs
; 21(7)2023 Jun 28.
Artigo
Inglês
| MEDLINE | ID: mdl-37504912
5.
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder.
Am J Hum Genet
; 105(5): 1048-1056, 2019 11 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31668703
6.
Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking.
Brain
; 144(3): 769-780, 2021 04 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33764426
7.
Association between plant and animal proteins intake with lipid profile and anthropometric indices: A cross-sectional study.
Nutr Health
; : 2601060221104311, 2022 Jun 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35656771
8.
Facial and Abducens Nerve Palsies Following COVID-19 Vaccination: Report of Two Cases.
Neuroophthalmology
; 46(3): 203-206, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35574171
9.
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy.
Brain
; 143(5): 1447-1461, 2020 05 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32282878
10.
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination.
Brain
; 142(10): 2948-2964, 2019 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31501903
11.
MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome).
J Med Genet
; 56(5): 332-339, 2019 05.
Artigo
Inglês
| MEDLINE | ID: mdl-30487245
12.
An analysis of factors associated with graft topographic outcomes after deep anterior lamellar keratoplasty.
Int Ophthalmol
; 40(10): 2449-2459, 2020 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-32424528
13.
Outcomes of big-bubble deep anterior lamellar keratoplasty for pediatric keratoconus.
Int Ophthalmol
; 40(5): 1253-1259, 2020 May.
Artigo
Inglês
| MEDLINE | ID: mdl-31974823
14.
Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function.
Hum Mutat
; 40(3): 267-280, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30520571
15.
Configuration of recipient corneal cut after mechanical trephination in keratoconus.
Int Ophthalmol
; 39(11): 2553-2559, 2019 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-30968329
16.
Expression of Pluripotency Markers, SOX2 and OCT4, in Pterygium Development.
Crit Rev Eukaryot Gene Expr
; 28(2): 155-162, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-30055542
17.
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.
Hum Genet
; 137(6-7): 479-486, 2018 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-29982980
18.
Expanding the clinical phenotype of IARS2-related mitochondrial disease.
BMC Med Genet
; 19(1): 196, 2018 11 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30419932
19.
Greater adherence to the dietary approaches to stop hypertension (DASH) dietary pattern is associated with lower blood pressure in healthy Iranian primary school children.
Eur J Nutr
; 57(4): 1449-1458, 2018 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-28321547
20.
A Western dietary pattern is associated with higher blood pressure in Iranian adolescents.
Eur J Nutr
; 56(1): 399-408, 2017 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26534856