J. Khan

ANTITHROMBIN III LEVEL IN PATIENTS OF β-THALASSEMIA: A CROSS-SECTIONAL STUDY

A. Saad, J. Khan, Tahir Khan, 2018 .

The effect of spironolactone on cardiovascular function and markers of fibrosis in people at increased risk of developing heart failure: the heart ‘OMics’ in AGEing (HOMAGE) randomized clinical trial

S. Heymans, J. Staessen, J. Cleland, 2020, European heart journal.

Frequency of acquired anti-thrombin III deficiency in patients with disseminated intravascular coagulation

A. Raza, Sadia Taj, A. Saad, 2019 .

A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.

Qing Zhou, Susan Moir, Matilda Katan, 2012, American journal of human genetics.

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.

Smita Y. Patel, Steven M Holland, M. Raffeld, 2011, Blood.

Proteomic and Mechanistic Analysis of Spironolactone in Patients at Risk for HF.

S. Heymans, J. Staessen, F. Zannad, 2020, JACC. Heart failure.

Pharmacologic Profile of the Adnectin BMS-962476, a Small Protein Biologic Alternative to PCSK9 Antibodies for Low-Density Lipoprotein Lowering

Doree Sitkoff, Daniel Meyers, R. Parker, 2014, The Journal of Pharmacology and Experimental Therapeutics.

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.

Smita Y. Patel, M. Raffeld, S. Pittaluga, 2011, Blood.

A study of the association of leukopenia with disease severity and mortality in patients diagnosed with COVID-19

A. Saini, A. Parasher, Abhinav Aggarwal, 2020 .