E-LIB Suche - Ergebnisse für: Amos, Samuel F.

1

Structural diversity, computational outputs, and supramolec..:

Shotonwa, Ibukun O. ; Osifeko, Olawale L. ; Amos, Samuel F....
Journal of Molecular Structure. 1310 (2024) - p. 138242 , 2024

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

2

Molecular Surveillance Identifies Multiple Transmissions of..:

International Typhoid Consortium ; Wong, Vanessa K. ; Holt, Kathryn E....
PLOS Neglected Tropical Diseases. 10 (2016) 9 - p. e0004781 , 2016

Link: https://doi.org/10.1371/..

3

Contributors:

, In: Transplantation of the Liver,

Abhinandana, Anantharaju ; Abu-Elmagd, Kareem ; Alonso, Estella M.... - p. v-xviii , 2005

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

4

Contributors:

, In: Surgical Research,

Abbott, William M. ; Abcouwer, Steve F. ; Adzick, N. Scott... - p. xix-xxv , 2001

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

5

Corrected TIMI frame counts correlate with stenosis severit..:

Amos, David J. ; French, John K. ; Andrews, Jacqueline...
American Heart Journal. 141 (2001) 4 - p. 586-591 , 2001

Link: https://doi.org/10.1067/..

6

Nonsyndromic cleft lip and palate is not associated with ca..:

Steinwachs, Ellen F. ; Amos, Chris ; Johnston, Dennis...
American Journal of Medical Genetics. 90 (2000) 1 - p. 17-24 , 2000

Link: https://doi.org/10.1002/..

7

Genetic epilepsy with febrile seizures plus: Refining the s..:

Zhang, Yue-Hua ; Burgess, Rosemary ; Malone, Jodie P....
Neurology. 89 (2017) 12 - p. 1210-1219 , 2017

Link: https://doi.org/10.1212/..

8

Seizures as presenting and prominent symptom in chorea‐acan..:

Benninger, Felix ; Afawi, Zaid ; Korczyn, Amos D....
Epilepsia. 57 (2016) 4 - p. 549-556 , 2016

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

9

Familial neonatal seizures in 36 families: Clinical and gen..:

Grinton, Bronwyn E. ; Heron, Sarah E. ; Pelekanos, James T....
Epilepsia. 56 (2015) 7 - p. 1071-1080 , 2015

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

10

Mutation of the nuclear lamin geneLMNB2in progressive myocl..:

Damiano, John A. ; Afawi, Zaid ; Bahlo, Melanie...
Human Molecular Genetics. 24 (2015) 16 - p. 4483-4490 , 2015

Link: https://doi.org/10.1093/..

11

TBC1D24 mutation associated with focal epilepsy, cognitive ..:

Afawi, Zaid ; Mandelstam, Simone ; Korczyn, Amos D....
Epilepsy Research. 105 (2013) 1-2 - p. 240-244 , 2013

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

12

Hybrid multi micropattern gaseous photomultiplier for detec..:

Duval, Samuel ; Arazi, Lior ; Breskin, Amos...
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. 695 (2012) - p. 163-167 , 2012

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

13

Missense mutations in the sodium-gated potassium channel ge..:

Heron, Sarah E ; Smith, Katherine R ; Bahlo, Melanie...
Nature Genetics. 44 (2012) 11 - p. 1188-1190 , 2012

Link: https://doi.org/10.1038/..

14

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy an..:

Heron, Sarah E. ; Grinton, Bronwyn E. ; Kivity, Sara...
The American Journal of Human Genetics. 90 (2012) 1 - p. 152-160 , 2012

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

15

Mild adolescent/adult onset epilepsy and paroxysmal exercis..:

Afawi, Zaid ; Suls, Arvid ; Ekstein, Dana...
Epilepsia. 51 (2010) 12 - p. 2466-2469 , 2010

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