Pakistan (PK)

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

Leptin and Associated Mediators of Immunometabolic Signaling: Novel Molecular Outcome Measures for Neurostimulation to Treat Chronic Pain (2019) Kinfe TM, Buchfelder M, Chaudhry SR, Chakravarthy KV, Deer TR, Russo M, Georgius P, et al. Journal article, Review article The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome (2019) Berner D, Hoja U, Zenkel M, Ross JJ, Uebe S, Paoli D, Frezzotti P, et al. Journal article Advances in orally-delivered pH-sensitive nanocarrier systems; an optimistic approach for the treatment of inflammatory bowel disease (2019) Zeeshan M, Ali H, Khan S, Khan SA, Weigmann B Journal article, Review article Trees record changes of the temperate glaciers on the Tibetan Plateau: Potential and uncertainty (2019) Zhu H, Shao X, Zhang H, Asad F, Sigdel SR, Huang R, Li Y, et al. Journal article Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis (2019) Amar A, Majmundar AJ, Ullah I, Afzal A, Braun DA, Shril S, Daga A, et al. Journal article Aluminum and aluminum nitrides effect on nucleation sites in micro-alloyed steel (2019) Abro SH, Chandio A, Siddiqui MA, Channa IA Journal article Unilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome profiling. (2019) Kinfe TM, Asif M, Chakravarthy KV, Deer TR, Kramer JM, Yearwood TL, Hurlemann R, et al. Journal article Establishment of Reference Intervals for Alkaline Phosphatase in Pakistani Children Using a Data Mining Approach (2019) Ahmed S, Zierk J, Khan AH Journal article De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder (2019) Mirzaa GM, Chong JX, Piton A, Popp B, Foss K, Guo H, Harripaul R, et al. Journal article Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia (2019) Iqbal Z, Tawamie H, Ba W, Reis A, Halak BA, Sticht H, Uebe S, et al. Journal article