Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Abeer Almehdar"'
Autor:
Ahmad Alahmad, Alessia Nasca, Juliana Heidler, Kyle Thompson, Monika Oláhová, Andrea Legati, Eleonora Lamantea, Jana Meisterknecht, Manuela Spagnolo, Langping He, Seham Alameer, Fahad Hakami, Abeer Almehdar, Anna Ardissone, Charlotte L Alston, Robert McFarland, Ilka Wittig, Daniele Ghezzi, Robert W Taylor
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 11, Pp 1-14 (2020)
Abstract Leigh syndrome is a progressive neurodegenerative disorder, most commonly observed in paediatric mitochondrial disease, and is often associated with pathogenic variants in complex I structural subunits or assembly factors resulting in isolat
Externí odkaz:
https://doaj.org/article/8060cfefccbf4f1692d0ea57083765cf
Autor:
Alaa Samkari, Jubara Alallah, Hammam Kandil, Reema M. Badros, Aouhoud M. Ali, Mansour Qurashi, Abeer Almehdar
Publikováno v:
NeoReviews. 22:e689-e692
A male neonate is born at 38 weeks’ gestation via elective cesarean section to a 28-year-old gravida 4, para 3 woman. The neonate’s parents are first-degree cousins without a significant family history. The maternal history is unremarkable. She r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac00f698e722e1c567de69809eba8601
https://doi.org/10.1542/neo.22-10-e689
https://doi.org/10.1542/neo.22-10-e689
Publikováno v:
Current Cancer Therapy Reviews. 16:276-291
Hepatoblastoma (HB) is the most common primary malignant hepatic tumor of childhood and, occurring predominantly in the first two years of life. Approximately 100 cases are diagnosed every year in the United States of America. The management of HB ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca302f34fcf95b8491a9eaa581a42049
https://doi.org/10.2174/1573394716666200206103826
https://doi.org/10.2174/1573394716666200206103826
Autor:
Saeed M. Bassem, Daniah E. Abdullatif, Abdullah Baothman, Waheed A. AlZhrani, Khursheed D. Ahmed, Abeer Almehdar, Naglla Elimam
Publikováno v:
Saudi medical journal. 42(12)
Objectives: To retrospectively review a small series of infant neuroblastoma (NBL) in a single Saudi medical institution over 10 years, including their presentation, management, and outcomes. Methods: Fifty-three subjects aged 0 to 14 years with prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::437428c55dd5edca7e984b5370a2e8d7
https://pubmed.ncbi.nlm.nih.gov/34853141
https://pubmed.ncbi.nlm.nih.gov/34853141
Publikováno v:
Hematology (Amsterdam, Netherlands). 26(1)
Ataxia telangiectasia (A-T) is a rare childhood autosomal recessive neurodegenerative chromosomalin stability disorder. It is characterized by high risk of hematological malignancies with T-cell phenotype being the most common, which can present firs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f34a90f1c8384d6fd41fe08c27f81b
https://pubmed.ncbi.nlm.nih.gov/33843495
https://pubmed.ncbi.nlm.nih.gov/33843495
Ataxia telangiectasia (A-T) is a rare childhood autosomal recessive neurodegenerative chromosomal instability disorder. It is characterized by high risk of hematological malignancies with T-cell phenotype being the most common, which can present firs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0584ff3c2c88d59f30024f8c4928b7cc
https://doi.org/10.22541/au.160610415.55719975/v1
https://doi.org/10.22541/au.160610415.55719975/v1
Autor:
Eleonora Lamantea, Robert McFarland, Langping He, Alessia Nasca, Anna Ardissone, Daniele Ghezzi, Kyle Thompson, Andrea Legati, Charlotte L. Alston, Seham Alameer, Robert W. Taylor, Fahad Hakami, Monika Oláhová, Abeer Almehdar, Juliana Heidler, Ahmad Alahmad, Ilka Wittig, Jana Meisterknecht, Manuela Spagnolo
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 11, Pp n/a-n/a (2020)
EMBO Molecular Medicine
EMBO Molecular Medicine
Leigh syndrome is a progressive neurodegenerative disorder, most commonly observed in paediatric mitochondrial disease, and is often associated with pathogenic variants in complex I structural subunits or assembly factors resulting in isolated respir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ada59065e8cb51941b837c36a5a138b
https://doi.org/10.15252/emmm.202012619
https://doi.org/10.15252/emmm.202012619
Publikováno v:
Cureus
Duodenal diverticulosis (DD) is a rare disease in children, and its etiology is unknown. Here, we report a 13-year-old boy with severe abdominal pain. A diagnosis of DD was made based on clinical and image findings. He responds to analgesic, antibiot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e536de7fef72aafb934bbd41fcb582
http://europepmc.org/articles/PMC7580970
http://europepmc.org/articles/PMC7580970
Autor:
Wasil Jastaniah, Mohammed Burhan Abrar, Naglla Elimam, Abeer Almehdar, Shaker Abdullah, Khalid Abdalla
Publikováno v:
Child's Nervous System. 34:861-870
Treatment modality impacts outcome of childhood low-grade glioma (LGG). Optimizing management in developing countries can be challenging. This study evaluates the clinical characteristics, treatment, and factors influencing outcome of childhood LGG i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b303beb29a2176c82c531135f3df6ef7
https://doi.org/10.1007/s00381-018-3729-6
https://doi.org/10.1007/s00381-018-3729-6
Publikováno v:
Topics in magnetic resonance imaging : TMRI. 27(4)
Peroxisomes play vital roles in a broad spectrum of cellular metabolic pathways. Defects in genes encoding peroxisomal proteins can result in a wide array of disorders, depending upon the metabolic pathways affected. These disorders can be broadly cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52898b24d4309bcf6715711324cb8489
https://pubmed.ncbi.nlm.nih.gov/30086110
https://pubmed.ncbi.nlm.nih.gov/30086110