Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Mie Rizig"'
Autor:
Nourhan Shebl, Shaimaa El-Jaafary, Ayman A. Saeed, Passent Elkafrawy, Amr El-Sayed, Samir Shamma, Rasha Elnemr, Jaidaa Mekky, Lobna A. Mohamed, Omar Kittaneh, Hassan El-Fawal, Mie Rizig, Mohamed Salama
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Introduction: Parkinson’s disease (PD) is the most common motor neurodegenerative disease worldwide. Given the complexity of PD etiology and the different metabolic derangements correlated to the disease, metabolomics profiling of patients is a hel
Externí odkaz:
https://doaj.org/article/ab3166e376eb444794d5c117fb209b2c
Autor:
Njideka U. Okubadejo, Olaitan Okunoye, Oluwadamilola O. Ojo, Babawale Arabambi, Rufus O. Akinyemi, Godwin O. Osaigbovo, Sani A. Abubakar, Emmanuel U. Iwuozo, Kolawole W. Wahab, Osigwe P. Agabi, Uchechi Agulanna, Frank A. Imarhiagbe, Oladunni V. Abiodun, Charles O. Achoru, Akintunde A. Adebowale, Olaleye Adeniji, John E. Akpekpe, Mohammed W. Ali, Ifeyinwa Ani-Osheku, Ohwotemu Arigbodi, Salisu A. Balarabe, Abiodun H. Bello, Oluchi S. Ekenze, Cyril O. Erameh, Temitope H. Farombi, Michael B. Fawale, Morenikeji A. Komolafe, Paul O. Nwani, Ernest O. Nwazor, Yakub Nyandaiti, Emmanuel E. Obehighe, Yahaya O. Obiabo, Olanike A. Odeniyi, Francis E. Odiase, Francis I. Ojini, Gerald A. Onwuegbuzie, Nosakhare Osemwegie, Olajumoke O. Oshinaike, Folajimi M. Otubogun, Shyngle I. Oyakhire, Funlola T. Taiwo, Uduak E. Williams, Simon Ozomma, Yusuf Zubair, Dena Hernandez, Sara Bandres-Ciga, Cornelis Blauwendraat, Andrew Singleton, Henry Houlden, John Hardy, Mie Rizig
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract The relationship between APOE polymorphisms and Parkinson’s disease (PD) in black Africans has not been previously investigated. We evaluated the association between APOE polymorphic variability and self-declared cognition in 1100 Nigerian
Externí odkaz:
https://doaj.org/article/df88b4a766664abd8c83b1ebb93f0d3b
Autor:
Alexandra Lackova, Christian Beetz, Sebastian Oppermann, Peter Bauer, Petra Pavelekova, Tatiana Lorincova, Miriam Ostrozovicova, Kristina Kulcsarova, Jana Cobejova, Martin Cobej, Petra Levicka, Simona Liesenerova, Daniela Sendekova, Viktoria Sukovska, Zuzana Gdovinova, Vladimir Han, Mie Rizig, Henry Houlden, Matej Skorvanek
Publikováno v:
Parkinson's Disease, Vol 2022 (2022)
Background. An increased prevalence of Parkinson’s disease (PD) disease has been previously reported in subjects with Fabry disease (FD) carrying alpha-galactosidase (GLA) mutations and their first-line relatives. Moreover, decreased alpha-galactos
Externí odkaz:
https://doaj.org/article/735f7ce759224bf6b7c29b9c1c8373fb
Autor:
Rauan Kaiyrzhanov, Akbota Aitkulova, Chingiz Shashkin, Nazira Zharkinbekova, Mie Rizig, Elena Zholdybayeva, Zharkyn Jarmukhanov, Vadim Akhmetzhanov, Gulnaz Kaishibayeva, Talgat Khaibullin, Altynay Karimova, Serik Akshulakov, Askhat Bralov, Nurlan Kissamedenov, Zhanar Seidinova, Anjela Taskinbayeva, Aliya Muratbaikyzy, Henry Houlden
Publikováno v:
Parkinson's Disease, Vol 2020 (2020)
Background. LRRK2 mutations have emerged as the most prevalent and potentially treatable determinants of Parkinson’s disease (PD). Peculiar geographic distribution of these mutations has triggered an interest in genotyping PD cohorts of different e
Externí odkaz:
https://doaj.org/article/e1290314fb6d4c18a782d814d7b74bc4
Autor:
Rauan Kaiyrzhanov, Mie Rizig, Akbota Aitkulova, Nazira Zharkinbekova, Chingiz Shashkin, Gulnaz Kaishibayeva, Altynay Karimova, Talgat Khaibullin, Dinara Sadykova, Manizha Ganieva, Khurshidakhon Rasulova, Henry Houlden
Publikováno v:
Parkinson's Disease, Vol 2019 (2019)
Our understanding of Parkinson’s disease (PD) has significantly accelerated over the last few years, but predominant advances have been made in developed, Western countries. Little is known about PD in the Central Asian (CA) and Transcaucasian (TC)
Externí odkaz:
https://doaj.org/article/e3f28fd22b6a4a5aa21ba47e3b83688a
Autor:
Njideka U Okubadejo, Mie Rizig, Oluwadamilola O Ojo, Hallgeir Jonvik, Olajumoke Oshinaike, Emmeline Brown, Henry Houlden
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0207984 (2018)
To date the LRRK2 p.G2019S mutation remains the most common genetic cause of Parkinson disease (PD) worldwide. It accounts for up to 6% of familial and approximately 1.5% of sporadic cases. LRRK2 has a kinase enzymatic domain which provides an attrac
Externí odkaz:
https://doaj.org/article/121dd4b5fc6b44b6a1967b9acfe3815a
Publikováno v:
Sunday, April 23.
Autor:
Olaitan Okunoye, Oluwadamilola Ojo, Oladunni Abiodun, Sani Abubakar, Charles Achoru, Olaleye Adeniji, Osigwe Agabi, Uchechi Agulanna, Rufus Akinyemi, Mohammed Ali, Ifeyinwa Ani-Osheku, Owotemu Arigbodi, Abiodun Bello, Cyril Erameh, Temitope Farombi, Michael Fawale, Frank Imarhiagbe, Emmanuel Iwuozo, Morenikeji Komolafe, Paul Nwani, Ernest Nwazor, Yakub Nyandaiti, Yahaya Obiabo, Olanike Odeniyi, Francis Odiase, Francis Ojini, Gerald Onwuegbuzie, Godwin Osaigbovo, Nosakhare Osemwegie, Olajumoke Oshinaike, Folajimi Otubogun, Shyngle Oyakhire, Simon Ozomma, Sarah Samuel, Funmilola Taiwo, Kolawole Wahab, Yusuf Zubair, Dena Hernandez, Sara Bandres-Ciga, Cornelis Blauwendraat, Andrew Singleton, Henry Houlden, John Hardy, Mie Rizig, Njideka Okubadejo
Publikováno v:
medRxiv
BackgroundThe microtubule-associated protein tau (MAPT) gene is critical because of its putative role in the causal pathway of neurodegenerative diseases including Parkinson’s disease (PD). However, there is a lack of clarity regarding the link bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb3c8d7849c2aa2ce20a16eb9a65233b
https://doi.org/10.1101/2023.03.24.23287684
https://doi.org/10.1101/2023.03.24.23287684
Autor:
Cyril O. Erameh, Temitope Farombi, Uchechi Agulanna, Funlola T. Taiwo, Ohwotemu Arigbodi, Morenikeji Komolafe, John E. Akpekpe, Babawale Arabambi, Nosakhare Osemwegie, Emmanuel E. Obehighe, Babatunde Ademiluyi, Olajumoke Oshinaike, SA Abubakar, Charles O. Achoru, Abiodun H Bello, Akintunde A Adebowale, Njideka U Okubadejo, Rufus Akinyemi, Shyngle I. Oyakhire, Kolawole Wahab, E U Iwuozo, Olanike A. Odeniyi, Bertha C. Ekeh, Michael B. Fawale, Ifeyinwa Ani-Osheku, Gerald A. Onwuegbuzie, Oladunni V. Abiodun, Mie Rizig, Frank Aiwansoba Imarhiagbe, Yakub Wilberforce Nyandaiti, Franklin O Dike, Ernest O. Nwazor, Folajimi M. Otubogun, Paul O Nwani, Yusuf A. Zubair, Salisu A. Balarabe, Oluwadamilola O. Ojo, Yahaya Obiabo, Godwin Osaigbovo, O. S. Ekenze, Francis E Odiase, Mohammed W. Ali, Francis I Ojini, Osigwe P. Agabi, Abiodun J. Kehinde, Christian E. Agu, U. E. Williams, Olaleye Adeniji
Publikováno v:
Mov Disord Clin Pract
BACKGROUND: Data on non‐motor symptoms (NMS) in black Africans with Parkinson's disease (PD) are sparse. OBJECTIVE: To describe the profile of NMS in the Nigeria PD Registry (NPDR) cohort and explore the relationship between NMS and PD motor phenot
Autor:
Maouly Fall, Ibrahim M. Dardare, Alassane M. Diop, Michel A. Pelagie, Jamil Kahwagi, Ghislain C. Dechacus, Ndiaga M. Gaye, Mie Rizig, Ngor S. Diagne, Moustapha Ndiaye, Amadou G. Diop
Publikováno v:
Parkinsonism & Related Disorders. 98:13-15
Movement disorders have different prevalence in different regions and they are little studied in Africa.Evaluate the prevalence and determine the spectrum of movement disorders in the first specialized center in Senegal.It was a prospective study ove