E-LIB Suche - Ergebnisse für: Simpson, MA

1

Elucidating the molecular genetic basis of cluster headache..:

Southgate, L ; Scollen, S ; He, W...
The Journal of Headache and Pain. 14 (2013) S1 - p. , 2013

Link: https://doi.org/10.1186/..

2

Elucidating the molecular genetic basis of cluster headache..:

Southgate, L ; Scollen, S ; He, W...
The Journal of Headache and Pain. 1 (2013) Suppl 1 - p. P34 , 2013

Link: https://doi.org/10.1186/..

3

Massively parallel sequencing and identification of genes f..:

Ostergaard, P ; Simpson, MA ; Jeffery, S
Clinical Genetics. 80 (2011) 2 - p. 110-116 , 2011

Link: https://doi.org/10.1111/..

4

Mutations in FAM20C also identified in non‐lethal osteoscle..:

Simpson, MA ; Scheuerle, A ; Hurst, J...
Clinical Genetics. 75 (2009) 3 - p. 271-276 , 2009

Link: https://doi.org/10.1111/..

5

Novel mutations in the pejvakin gene are associated with au..:

Hashemzadeh Chaleshtori, M ; Simpson, MA ; Farrokhi, E...
Clinical Genetics. 72 (2007) 3 - p. 261-263 , 2007

Link: https://doi.org/10.1111/..

6

Serum electrolytes can promote hydroxyl radical-initiated b..:

Komaki, Yukako ; Simpson, Adam M-A. ; Choe, Jong Kwon...
Free Radical Biology and Medicine. 141 (2019) - p. 475-482 , 2019

Link: https://doi.org/10.1016/..

7

Relationships between self-help health organizations and pr..:

Simpson MA RGN SCM, Rosemary Graham
Health & Social Care in the Community. 4 (2007) 6 - p. 359-370 , 2007

Link: https://doi.org/10.1111/..

8

Comparative Genetic Analysis of Psoriatic Arthritis and Pso..:

Soomro, M ; Stadler, M ; Dand, N...
https://eprints.whiterose.ac.uk/191095/1/Arthritis%20%20%20Rheumatology%20-%202022%20-%20Soomro%20-%20Comparative%20Genetic%20Analysis%20of%20Psoriatic%20Arthritis%20and%20Psoriasis%20for%20the.pdf. , 2022

Link: https://eprints.whiteros..

9

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelop..:

Reid, KM ; Spaull, R ; Salian, S...
https://discovery.ucl.ac.uk/id/eprint/10153087/1/Movement%20Disorders%20-%202022%20-%20Reid%20-%20MED27%20%20SLC6A7%20%20and%20MPPE1%20Variants%20in%20a%20Complex%20Neurodevelopmental%20Disorder%20with%20Severe.pdf. , 2022

Link: https://discovery.ucl.ac..

10

100,000 Genomes Pilot on Rare-Disease Diagnosis in Health C..:

100, 000 Genomes Project Pilot Investigators ; Smedley, D ; Smith, KR...
https://discovery.ucl.ac.uk/id/eprint/10138417/1/nejmoa2035790.pdf. , 2021

Link: https://discovery.ucl.ac..

11

Confirmation of Cause of Death Via Comprehensive Autopsy an..:

Chahal, CAA ; Tester, DJ ; Fayyaz, AU...
https://openaccess.sgul.ac.uk/id/eprint/113892/1/JAHA.121.021170.pdf. , 2021

Link: https://openaccess.sgul...

12

Coagulation Factor XIII-A Subunit Missense Mutation in the ..:

Supsrisunjai, C ; Hsu, C-K ; Michael, M...
https://eprints.whiterose.ac.uk/151669/1/Supsrisunjai%20et%20al,%202019.pdf. , 2020

Link: https://eprints.whiteros..

13

Bi-allelic loss-of-function CACNA1B mutations in progressiv..:

Gorman, KM ; Meyer, E ; Grozeva, D...
doi:10.1016/j.ajhg.2019.03.005. , 2019

Link: https://doi.org/10.1016/..

14

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressiv..:

Gorman, KM ; Meyer, E ; Grozeva, D...
https://discovery.ucl.ac.uk/id/eprint/10074594/1/Cross_AJHG-D-18-00798R2-final.pdf. , 2019

Link: https://discovery.ucl.ac..

15

Mitochondria function associated genes contribute to Parkin..:

Billingsley, KJ ; Barbosa, IA ; Bandres-Ciga, S...
NPJ PARKINSONS DISEASE. , 2019

Link: https://qmro.qmul.ac.uk/..