Detalhe da pesquisa
1.
Association of serum protein electrophoresis with clinicopathological characteristics and its prognostic relevance in chronic lymphocytic leukaemia patients.
J Pak Med Assoc
; 74(4): 711-718, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38751267
2.
Detection of Partially Structural Collapse Using Long-Term Small Displacement Data from Satellite Images.
Sensors (Basel)
; 22(13)2022 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35808455
3.
Association of early donor chimerism status with survival outcomes in post allogeneic haematopoietic stem cell transplant patients of nonmalignant diseases.
J Pak Med Assoc
; 72(3): 464-470, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35320226
4.
Electrically controlled 1 × 2 tunable switch using a phase change material embedded silicon microring.
Appl Opt
; 60(13): 3559-3568, 2021 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33983284
5.
Refining the role of phenology in regulating gross ecosystem productivity across European peatlands.
Glob Chang Biol
; 26(2): 876-887, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31686431
6.
Mid-infrared non-volatile silicon photonic switches using nanoscale Ge2Sb2Te5 embedded in silicon-on-insulator waveguides.
Nanotechnology
; 31(11): 115207, 2020 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31751966
7.
European In-Situ Snow Measurements: Practices and Purposes.
Sensors (Basel)
; 18(7)2018 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29932447
8.
The effectiveness of script training to restore lost communication in a patient with Broca's aphasia.
J Pak Med Assoc
; 68(7): 1070-1075, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30317304
9.
Recurrent Kimura Disease of the Inner Canthus With No Lymphadenopathy.
Ophthalmic Plast Reconstr Surg
; 33(3S Suppl 1): S45-S47, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-26020715
10.
Rare ß-Globin Gene Mutations in Pakistan.
Hemoglobin
; 41(2): 100-103, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28670940
11.
Bilingual Aphasia Test in Urdu and its Clinical Implications.
Pak J Med Sci
; 37(5): 1545-1546, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34475946
12.
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.
BMC Med Genet
; 16: 41, 2015 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26104215
13.
DRY TAP: A DIAGNOSTIC ALERT FOR UNDERLYING BONE MARROW PATHOLOGY.
J Ayub Med Coll Abbottabad
; 27(1): 120-3, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26182755
14.
Frequency of hereditary thrombophilia in women with recurrent pregnancy loss in Northern Pakistan.
J Obstet Gynaecol Res
; 40(6): 1561-6, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24888916
15.
High prevalence of protein C, protein S, antithrombin deficiency, and Factor V Leiden mutation as a cause of hereditary thrombophilia in patients of venous thromboembolism and cerebrovascular accident.
Pak J Med Sci
; 30(6): 1323-6, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25674132
16.
Spectrum of intra-ocular foreign bodies and the outcome of their management in Brunei Darussalam.
Int Ophthalmol
; 33(3): 277-84, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23229396
17.
Prevalence of various mutations in beta thalassaemia and its association with haematological parameters.
J Pak Med Assoc
; 62(1): 40-3, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22352100
18.
Guidelines on the laboratory diagnosis of congenital bleeding disorders in Pakistan.
J Pak Med Assoc
; 62(5): 477-86, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22755314
19.
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease.
Genes (Basel)
; 13(6)2022 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35741733
20.
Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families.
Hum Genet
; 129(4): 419-24, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21188418