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Practical Neurology
|
March 31, 2021
Don't forget the fornix
Maurice Sidra, Louise Hattingh, Hawraman Ramadan
Archives of Disease in Childhood. Education and Practice Edition
|
April 6, 2019
Long lines and atypical anatomy
Katherine J Pettinger, Alexander I C Wordie, Chris J Vas, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
November 14, 2016
Screening, characterisation and prevention of Hepatitis B virus (HBV) co-infection in HIV-positive children in South Africa
Pieter Jooste, Anriette van Zyl, Emily Adland, et al.
BMC Medicine
|
February 22, 2019
HBV vaccination and PMTCT as elimination tools in the presence of HIV: insights from a clinical cohort and dynamic model
Anna L McNaughton, José Lourenço, Louise Hattingh, et al.
American Journal of Human Genetics
|
November 10, 2009
Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia
Mohammad R Abdollahi, Ewan Morrison, Tamara Sirey, et al.
Wellcome Open Research
|
May 13, 2017
PARV4 prevalence, phylogeny, immunology and coinfection with HIV, HBV and HCV in a multicentre African cohort
Colin P Sharp, William F Gregory, Louise Hattingh, et al.
European Radiology
|
January 31, 2026
Rib fracture diagnosis in suspected abuse: Computed tomography or radiographs (RECEPTOR)? A multicentre diagnostic accuracy observational study
Nasser M Alzahrani, Michael Paddock, Annmarie Jeanes, et al.
European Radiology
|
April 2, 2026
Reply to the Letter to the Editor: Rib fracture diagnosis in suspected abuse-clinical and methodological considerations
Nasser Mohammed Alzahrani, Michael Paddock, Annmarie Jeanes, et al.
Human Molecular Genetics
|
December 12, 2017
DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport
Verity L Hartill, Glenn van de Hoek, Mitali P Patel, et al.
American Journal of Human Genetics
|
November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
Thi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Practical Neurology
|
March 31, 2021
Don't forget the fornix
Maurice Sidra, Louise Hattingh, Hawraman Ramadan
Archives of Disease in Childhood. Education and Practice Edition
|
April 6, 2019
Long lines and atypical anatomy
Katherine J Pettinger, Alexander I C Wordie, Chris J Vas, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
November 14, 2016
Screening, characterisation and prevention of Hepatitis B virus (HBV) co-infection in HIV-positive children in South Africa
Pieter Jooste, Anriette van Zyl, Emily Adland, et al.
BMC Medicine
|
February 22, 2019
HBV vaccination and PMTCT as elimination tools in the presence of HIV: insights from a clinical cohort and dynamic model
Anna L McNaughton, José Lourenço, Louise Hattingh, et al.
American Journal of Human Genetics
|
November 10, 2009
Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia
Mohammad R Abdollahi, Ewan Morrison, Tamara Sirey, et al.
Wellcome Open Research
|
May 13, 2017
PARV4 prevalence, phylogeny, immunology and coinfection with HIV, HBV and HCV in a multicentre African cohort
Colin P Sharp, William F Gregory, Louise Hattingh, et al.
European Radiology
|
January 31, 2026
Rib fracture diagnosis in suspected abuse: Computed tomography or radiographs (RECEPTOR)? A multicentre diagnostic accuracy observational study
Nasser M Alzahrani, Michael Paddock, Annmarie Jeanes, et al.
European Radiology
|
April 2, 2026
Reply to the Letter to the Editor: Rib fracture diagnosis in suspected abuse-clinical and methodological considerations
Nasser Mohammed Alzahrani, Michael Paddock, Annmarie Jeanes, et al.
Human Molecular Genetics
|
December 12, 2017
DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport
Verity L Hartill, Glenn van de Hoek, Mitali P Patel, et al.
American Journal of Human Genetics
|
November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
Thi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
Page
of 1