Suchergebnisse - "Khan, Amjad"

PubPharm (187)

1

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

2

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

3

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

4

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

5

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

6

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

enthalten in: Preprints.org | 2019

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

7

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

8

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

9

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

10

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

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