Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Salah A.D. Ebrahim"'
Autor:
Salah A.D. Ebrahim, Nada Emara, Anwar N. Mohamed, Mustapha Kandouz, Abdul Shukkur Ebrahim, Ali Raufi, Ayad Al-Katib, Feras Zaiem, Ali Gabali
Publikováno v:
Oncotarget. 11:148-160
Non-Hodgkin's lymphoma (NHL) is the most common hematological malignancy in the US. Many types remain incurable despite response to initial therapy and achievement of complete remission (CR). Advanced laboratory techniques like multicolor flow cytome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99ff8200577c91881d279d737505a1dd
https://doi.org/10.18632/oncotarget.27415
https://doi.org/10.18632/oncotarget.27415
Autor:
Karoline S. Puder, Mili Thakur, Bernard Gonik, Salah A.D. Ebrahim, Henry Adekola, Elena Bronshtein, Michael Hankerd
Publikováno v:
American Journal of Medical Genetics Part A. 176:1985-1990
Terminal deletions of the chromosome 6q27 region are rare genomic abnormalities, linked to specific brain malformations and other neurological phenotypes. Reported cases have variable sized genomic deletions that harbor several genes including the DL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732117a5beb3bc37ff361ac798bda65a
https://doi.org/10.1002/ajmg.a.40376
https://doi.org/10.1002/ajmg.a.40376
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 199-204 (2015)
Egyptian Journal of Medical Human Genetics; Vol 16, No 2 (2015); 199-204
Egyptian Journal of Medical Human Genetics; Vol 16, No 2 (2015); 199-204
We report on the molecular detection of two microduplications involving chromosomes Xp21.1–Xp21.2 and 17p12 in a 35-year-old female with clinical phenotype of Charcot–Marie–Tooth disease type 1A (CMT1A) documented by chromosomal microarray anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6da6990c96d4f09221a3f6e9bda36b70
http://www.sciencedirect.com/science/article/pii/S111086301400130X
http://www.sciencedirect.com/science/article/pii/S111086301400130X
Autor:
Pankaj Prasun, Michael Hankerd, Lalitha Sivaswamy, Salah A.D. Ebrahim, Lindsey Scussel, Melissa Kristofice
Publikováno v:
American Journal of Medical Genetics Part A. 164:1815-1820
Homozygous or compound heterozygous microdeletion of 15q13.3 region is a rare but clinically recognizable syndrome manifested by profound intellectual disability, muscular hypotonia, intractable seizures, and visual impairment. We identified a compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206ef67a7e5d828596ccbcf751c4d410
https://doi.org/10.1002/ajmg.a.36535
https://doi.org/10.1002/ajmg.a.36535
Autor:
Mustapha Kandouz, Ali Raufi, Salah A.D. Ebrahim, Ebrahim Abdul Shukkur, Ayad Al-Katib, Ali Gabali
Publikováno v:
Blood. 134:3970-3970
Non-Hodgkin's lymphoma (NHL) is the most common hematological malignancy in the US. Many types remain incurable despite response to initial therapy and achievement of complete remission (CR). Advanced laboratory techniques like multicolor flow cytome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88d61ac5dc933d888775a050fc43508e
https://doi.org/10.1182/blood-2019-130738
https://doi.org/10.1182/blood-2019-130738
Publikováno v:
Journal of Ultrasound in Medicine. 37:305-306
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0d48c757f519ad219fb170c43c6bb9e
https://doi.org/10.1002/jum.14328
https://doi.org/10.1002/jum.14328
Autor:
Cassandra K. Runke, Adewale Adeyinka, Janet Insko, Mark Micale, Salah A.D. Ebrahim, Daniel L. Van Dyke
Publikováno v:
Prenatal Diagnosis. 30:173-176
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f02dfa525bd143705f0188927c7a89f
https://doi.org/10.1002/pd.2429
https://doi.org/10.1002/pd.2429
Autor:
Prahlad Parajuli, Amro Aboukameel, Fazlul H. Sarkar, Seema Sethi, Sandeep Mittal, Lisa Polin, Sharon K. Michelhaugh, Anthony R. Guastella, Kaushik Varadarajan, Aliccia Bollig-Fischer, Ian M Zitron, Neil V. Klinger, Salah A.D. Ebrahim, Aamir Ahmad, Sam Kiousis
Publikováno v:
Journal of Translational Medicine
Background There is a paucity of effective therapies for recurrent/aggressive meningiomas. Establishment of improved in vitro and in vivo meningioma models will facilitate development and testing of novel therapeutic approaches. Methods A primary men
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4b06b58f34a54f23e7d61b51fbd9887
https://pubmed.ncbi.nlm.nih.gov/26174772
https://pubmed.ncbi.nlm.nih.gov/26174772
Publikováno v:
American Journal of Medical Genetics. :316-320
Ring chromosomes are thought to be the result of breakage in both arms of a chromosome, with fusion of the points of fracture and loss of the distal fragments. Another mechanism of ring formation is believed to be the simple fusion of chromosome ends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3496446559a209c44c7f3cf17cfa03c1
https://doi.org/10.1002/ajmg.a.30242
https://doi.org/10.1002/ajmg.a.30242
Autor:
Anthony Johnson, Mark P. Johnson, Ko Gyi, Sarah L. Hazan, Mark I. Evans, Baruch Feldman, Salah A.D. Ebrahim
Publikováno v:
American Journal of Medical Genetics. 90:233-238
This study is a prospective clinical trial with fluorescent in situ hybridization (FISH) as a "routine" test for prenatal detection of the most common aneuploidies in high-risk pregnancies. Since April 1996, FISH studies with multicolor, commercially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9a71329d9717607435b78c18114a3b4
https://doi.org/10.1002/(sici)1096-8628(20000131)90:3<233::aid-ajmg9>3.0.co
https://doi.org/10.1002/(sici)1096-8628(20000131)90:3<233::aid-ajmg9>3.0.co