W. Khan

发表

Loss-of-function mutations in ADCY3 cause monogenic severe obesity

M. U. Mirza, F. Tamanini, P. Froguel, 2018, Nature Genetics.

Role of motivational interviewing in type 1 Diabetes Mellitus with sub optimal glycemic control.

Erum Afzal, W. Khan, Sidrah Anjum, 2021 .

Cyanotic congenital heart disease: Impact on growth and endocrine functions.

H. Anwar-ul-Haq, A. Zulqarnain, W. Khan, 2021, The Professional Medical Journal.

Bacterial infection in wheezy children.

M. Saleem, W. Khan, A. Khurshid, 2021 .

Prevalence of psychosocial problems in children with and without epilepsy: A comparative cross-section study.

T. Ahmad, Erum Afzal, W. Khan, 2021 .

Identification and Computational Analysis of Novel TYR and SLC45A2 Gene Mutations in Pakistani Families With Identical Non-syndromic Oculocutaneous Albinism

N. Bibi, W. Ahmad, T. Khan, 2020, Frontiers in Genetics.

Etiology of ambiguous genitalia in newborns with XX karyotype: A cross-sectional observational study.

F. Rehman, A. Rehman, Erum Afzal, 2021 .

Endocrine complications in thalassemic children at a tertiary childcare hospital of South Punjab, Pakistan.

W. Khan, Sana Waqar, A. Khurshid, 2021, The Professional Medical Journal.

Frequency of Thyroid Dysfunction and Congenital Heart Defects in Subjects with Down Syndrome

Erum Afzal, W. Khan, M. Arshad, 2021, Journal of Rawalpindi Medical College.

Frequency of congenital hypothyroidism in healthy newborns.

W. Khan, A. Khurshid, Rooman Khalil, 2022 .

Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan

P. Froguel, A. Bonnefond, S. Lobbens, 2020, Diabetes.

Thyroid function disorders in low birth weight/preterm neonates admitted in NICU, Children Hospital Complex Multan.

I. Iqbal, A. Rehman, W. Khan, 2020 .

Saadia Khan, I. Ali, R. Arshad, 2019, The APRN and PA’s Complete Guide to Prescribing Drug Therapy.

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

A. Hattersley, S. Ellard, A. Gloyn, 2014, Human molecular genetics.

Glycemic status of infants of Diabetic mothers; a study at the Children’s Hospital and Institute of Child Health, Multan

I. Iqbal, A. Rehman, W. Khan, 2021 .

Evaluation of endocrine and cardiac complications in survivors of childhood acute lymphoblastic leukemia: A single center study from south Punjab.

Z. Ali, W. Khan, Sohail Arshad, 2021 .

Cardiac autonomic neuropathy in children and adolescents with Type 1 diabetes mellitus: Prevalence and relation to duration and control of diabetes.

S. Anjum, W. Khan, Sidrah Anjum, 2020, The Professional Medical Journal.

Biallelic mutations in P4HTM cause syndromic obesity.

John F. Trant, P. Froguel, A. Bonnefond, 2023, Diabetes.