Detalhe da pesquisa
1.
Genome-wide identification and characterization of wall-associated kinases, molecular docking and polysaccharide elicitation of monoterpenoid indole alkaloids in micro-propagated Catharanthus roseus.
J Plant Res
; 137(1): 125-142, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37962734
2.
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects.
Am J Hum Genet
; 107(2): 311-324, 2020 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32738225
3.
Outcomes of concomitant aortic valve procedures and left ventricular assist device implantation: A systematic review and meta-analysis.
Artif Organs
; 47(3): 470-480, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36537993
4.
Mammary analogue secretory carcinoma of the parotid gland: A rare tumour entity.
J Pak Med Assoc
; 73(2): 412-415, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36800741
5.
COMPARISON OF INTRAMUSCULAR VERSUS INTRAVENOUS KETAMINE FOR SEDATION IN CHILDREN UNDERGOING MAGNETIC RESONANCE IMAGING EXAMINATION.
Wiad Lek
; 76(1): 198-204, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36883510
6.
Biallelic variants in PSMB1 encoding the proteasome subunit ß6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature.
Hum Mol Genet
; 29(7): 1132-1143, 2020 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32129449
7.
Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency.
Hum Mol Genet
; 29(4): 618-623, 2020 03 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31903486
8.
Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features.
Am J Hum Genet
; 104(6): 1073-1087, 2019 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31079899
9.
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
Am J Hum Genet
; 105(5): 907-920, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31607425
10.
Resuscitative Endovascular Balloon Occlusion of Aorta Versus Aortic Cross-Clamping by Thoracotomy for Noncompressible Torso Hemorrhage: A Meta-Analysis.
J Surg Res
; 270: 252-260, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34715536
11.
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature.
Hum Mol Genet
; 28(6): 972-979, 2019 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30481285
12.
Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts.
Am J Hum Genet
; 103(4): 568-578, 2018 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30290152
13.
Effects of Anticoagulation on Patients With Intra-Aortic Balloon Pump-A Meta-Analysis of 19,427 Patients.
Am J Ther
; 31(3): e335-e338, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38227903
14.
Effects of Mavacamten Concomitant With Beta-Blockers on Patients With Hypertrophic Cardiomyopathy: A Meta-Analysis of Randomized Controlled Trials.
Am J Ther
; 2024 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38563758
15.
Evaluation of chromosomal abnormalities and Y chromosome microdeletion in infertile males of 10 families.
J Pak Med Assoc
; 69(4): 567-571, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31000864
16.
Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.
Genet Med
; 20(7): 778-784, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28837161
17.
Whole Genome Sequencing instead of Whole Exome Sequencing is required to identify the Genetic Causes of Polycystic Ovary Syndrome in Pakistani families.
Pak J Med Sci
; 34(3): 540-545, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30034412
18.
Investigation of Staphylococcus aureus, prevailing in the environment of Khyber Teaching Hospital, Peshawar, Pakistan.
Pak J Pharm Sci
; 31(2): 429-437, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29618431
19.
Evaluation of Non-Structural Protein-1(NS1) positive patients of 2013 dengue outbreak in Khyber Pakhtunkhwa, Pakistan.
Pak J Med Sci
; 33(1): 172-176, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28367194
20.
Diagnosis and phenotypic assessment of Pakistani Haemophilia B carriers.
Pak J Med Sci
; 33(3): 738-742, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28811805