Suchergebnisse - "Khan, Amjad"

PubPharm (549)

291

Retraction notice to "An epidemiological investigation of associated risk factors with equine influenza (H3N8) epidemic 2015-16 in Pakistan" [Acta Tropica 186 (2018) 63-68

enthalten in: Acta tropica | 2020

von Mushtaq, M. | Khan, A. | Ahmad, M. | +4

RetractionOf: Acta Trop. 2018 Oct;186:63-68. - PMID 30003906

292

The association of HIV and easy access to narcotics in Pakistan; calling drug policy makers

enthalten in: Journal of pharmaceutical policy and practice | 2019

von Mallhi, T. | Khan, Y. | Khan, A. | +3

293

Clinical Significance of Twinkling Artifact in the Diagnosis of Urinary Stones

enthalten in: Ultrasound in medicine & biology | 2019

von Bacha, R. | Manzoor, I. | Gilani, S. | +1

294

Correction to : Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

enthalten in: BMC medical genetics | 2019

von Khan, A. | Wang, R. | Han, S. | +6

ErratumFor: BMC Med Genet. 2019 Oct 29;20(1):166. - PMID 31664938

295

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

enthalten in: BMC medical genetics | 2019

von Khan, A. | Wang, R. | Han, S. | +6

296

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

enthalten in: BMC medical genetics | 2019

von Khan, A. | Wang, R. | Han, S. | +6

297

Myeloperoxidase as an Active Disease Biomarker: Its Recent Biochemical and Pathological Perspectives

enthalten in: Preprints.org | 2019

von Khan, A. | Alsahli, M. | Rahmani, A.

298

Platform for ergonomic intraoral photodynamic therapy using low-cost, modular 3D-printed components : Design, comfort and clinical evaluation

enthalten in: Scientific reports | 2019

von Mallidi, S. | Khan, A. | Liu, H. | +13

299

Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

enthalten in: BMC medical genetics | 2019

von Khan, A. | Wang, R. | Han, S. | +6

ErratumIn: BMC Med Genet. 2019 Dec 12;20(1):195. - PMID 31830914

300

Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

enthalten in: BMC medical genetics | 2019

von Khan, A. | Wang, R. | Han, S. | +6