Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sanaa Sharari"'
Autor:
Basma Haris, Ikhlak Ahmed, Najeeb Syed, Hakeem Almabrazi, Saras Saraswathi, Sara Al-Khawaga, Amira Saeed, Shihab Mundekkadan, Idris Mohammed, Sanaa Sharari, Iman Hawari, Noor Hamed, Houda Afyouni, Tasneem Abdel-Karim, Shayma Mohammed, Amel Khalifa, Maryam Al-Maadheed, Mahmoud Zyoud, Ahmed Shamekh, Ahmed Elawwa, Mohammed Y. Karim, Fawziya Al-Khalaf, Zohreh Tatari-Calderone, Goran Petrovski, Khalid Hussain
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract To describe the clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus (T1DM). Patients (0–18 years) with diabetes were recruited. Clinical data was collected, autoantibodies
Externí odkaz:
https://doaj.org/article/9405a71b574d47d8b7c24add1de0fccd
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 14, p 11326 (2023)
AD is the most common neurodegenerative disorder characterized by progressive memory impairment and cognitive deficits. The pathology of AD is still unclear; however, several studies have shown that the aggregation of the Aβ peptide in the CNS is an
Externí odkaz:
https://doaj.org/article/8ff04f73f0cd482595ebcada4910615d
Autor:
Sanaa Sharari, Mustapha Aouida, Idris Mohammed, Basma Haris, Ajaz Ahmad Bhat, Iman Hawari, Sabah Nisar, Igor Pavlovski, Kabir H. Biswas, Najeeb Syed, Selma Maacha, Jean-Charles Grivel, Maryam Saifaldeen, Johan Ericsson, Khalid Hussain
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized mainly by the accumulation of glycogen in the liver and kidney. It is inherited as an autosomal recessive disorder caused by mutations in the SLC2A2 g
Externí odkaz:
https://doaj.org/article/2d01c00c404341fe90e54f1b061e3e51
Autor:
Sanaa Sharari, Basirudeen Kabeer, Idris Mohammed, Basma Haris, Igor Pavlovski, Iman Hawari, Ajaz Ahmad Bhat, Mohammed Toufiq, Sara Tomei, Rebecca Mathew, Najeeb Syed, Sabah Nisar, Selma Maacha, Jean-Charles Grivel, Damien Chaussabel, Johan Ericsson, Khalid Hussain
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2114 (2022)
Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized by the accumulation of glycogen mainly in the liver. It is inherited in an autosomal recessive manner due to mutations in the SLC2A2 gene. SLC2A2 enco
Externí odkaz:
https://doaj.org/article/fdc507a460194407a6173afa34a196b8
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 17, p 6286 (2020)
Accumulation of glycogen in the kidney and liver is the main feature of Fanconi–Bickel Syndrome (FBS), a rare disorder of carbohydrate metabolism inherited in an autosomal recessive manner due to SLC2A2 gene mutations. Missense, nonsense, frame-shi
Externí odkaz:
https://doaj.org/article/ce3782237bfd4e2bba9a5a1ce4a7fdb3
Autor:
Sanaa Sharari, Mustapha Aouida, Idris Mohammed, Basma Haris, Ajaz Ahmad Bhat, Iman Hawari, Sabah Nisar, Igor Pavlovski, Kabir H. Biswas, Najeeb Syed, Selma Maacha, Jean-Charles Grivel, Maryam Saifaldeen, Johan Ericsson, Khalid Hussain
Publikováno v:
Frontiers in endocrinology. 13
Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized mainly by the accumulation of glycogen in the liver and kidney. It is inherited as an autosomal recessive disorder caused by mutations in the SLC2A2 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1bf5042df038e9a2ddc645ddb7dc10a
https://pubmed.ncbi.nlm.nih.gov/35663312
https://pubmed.ncbi.nlm.nih.gov/35663312
Autor:
Khalid Hussain, Fawziya Al-Khalaf, Idris Mohammed, Ikhlak Ahmed, Maryam Al-Maadheed, Goran Petrovski, Sara Al-Khawaga, Shayma Mohammed, Ahmed Shamekh, Najeeb Syed, Hakeem Almabrazi, Zohreh Tatari-Calderone, Saras Saraswathi, Iman Hawari, Amira Saeed, Noor Hamed, Shihab Mundekkadan, Houda Afyouni, Mohammed Yousuf Karim, Amel Khalifa, Basma Haris, Ahmed Elawwa, Sanaa Sharari, Mahmoud Zyoud, Tasneem Abdel-Karim
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
To describe the clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus (T1DM). Patients (0–18 years) with diabetes were recruited. Clinical data was collected, autoantibodies and c-pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eb2d2beb08818e2d4535337ce9136a1
http://europepmc.org/articles/PMC8460652
http://europepmc.org/articles/PMC8460652
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 6286, p 6286 (2020)
International Journal of Molecular Sciences, Vol 21, Iss 6286, p 6286 (2020)
Accumulation of glycogen in the kidney and liver is the main feature of Fanconi–Bickel Syndrome (FBS), a rare disorder of carbohydrate metabolism inherited in an autosomal recessive manner due to SLC2A2 gene mutations. Missense, nonsense, frame-shi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b47edce6f68a5ea25c3967696a3f70
https://pubmed.ncbi.nlm.nih.gov/32877990
https://pubmed.ncbi.nlm.nih.gov/32877990