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Journal of Medical Virology
|
February 21, 2024
A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma
Yuval Yogev, Moshe Schaffer, Mark Shlapobersky, et al.
Oncology Letters
|
April 5, 2019
The 1, 2, 3, 4 of carcinoid heart disease: Comprehensive cardiovascular imaging is the mainstay of complex surgical treatment
Dinu Valentin Balanescu, Teodora Donisan, Juan Lopez-Mattei, et al.
Journal of Medical Genetics
|
January 31, 2024
<i>ZNF142</i> mutation causes sex-dependent neurologic disorder
Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Zamir Shorer, et al.
Plos One
|
September 29, 2017
Efficacy and safety of sequential versus quadruple therapy as second-line treatment for helicobacter pylori infection-A randomized controlled trial
Daniela Munteanu, Ohad Etzion, Gil Ben-Yakov, et al.
Journal of Gastrointestinal Surgery : Official Journal of the Society for Surgery of the Alimentary Tract
|
September 17, 2016
Role of Fluorouracil, Doxorubicin, and Streptozocin Therapy in the Preoperative Treatment of Localized Pancreatic Neuroendocrine Tumors
Laura Prakash, Priya Bhosale, Jordan Cloyd, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 6, 2023
Limb girdle muscular disease caused by <i>HMGCR</i> mutation and statin myopathy treatable with mevalonolactone
Yuval Yogev, Zamir Shorer, Arie Koifman, et al.
Endocrine-Related Cancer
|
April 23, 2015
Phase I study of the anti-IGF1R antibody cixutumumab with everolimus and octreotide in advanced well-differentiated neuroendocrine tumors
Arvind Dasari, Alexandria Phan, Sanjay Gupta, et al.
American Journal of Medical Genetics. Part A
|
December 5, 2018
Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe
Ohad Wormser, Libe Gradstein, Einat Kadar, et al.
Journal of Medical Genetics
|
November 23, 2018
<i>SEC31A</i> mutation affects ER homeostasis, causing a neurological syndrome
Daniel Halperin, Rotem Kadir, Yonatan Perez, et al.
European Journal of Human Genetics : EJHG
|
May 11, 2017
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation
Yuval Yogev, Yonatan Perez, Iris Noyman, et al.
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Search research articles
Search
Showing results (31-40 of 57) with videos related to
Sort By:
Page
of 6
Journal of Medical Virology
|
February 21, 2024
A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma
Yuval Yogev, Moshe Schaffer, Mark Shlapobersky, et al.
Oncology Letters
|
April 5, 2019
The 1, 2, 3, 4 of carcinoid heart disease: Comprehensive cardiovascular imaging is the mainstay of complex surgical treatment
Dinu Valentin Balanescu, Teodora Donisan, Juan Lopez-Mattei, et al.
Journal of Medical Genetics
|
January 31, 2024
<i>ZNF142</i> mutation causes sex-dependent neurologic disorder
Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Zamir Shorer, et al.
Plos One
|
September 29, 2017
Efficacy and safety of sequential versus quadruple therapy as second-line treatment for helicobacter pylori infection-A randomized controlled trial
Daniela Munteanu, Ohad Etzion, Gil Ben-Yakov, et al.
Journal of Gastrointestinal Surgery : Official Journal of the Society for Surgery of the Alimentary Tract
|
September 17, 2016
Role of Fluorouracil, Doxorubicin, and Streptozocin Therapy in the Preoperative Treatment of Localized Pancreatic Neuroendocrine Tumors
Laura Prakash, Priya Bhosale, Jordan Cloyd, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 6, 2023
Limb girdle muscular disease caused by <i>HMGCR</i> mutation and statin myopathy treatable with mevalonolactone
Yuval Yogev, Zamir Shorer, Arie Koifman, et al.
Endocrine-Related Cancer
|
April 23, 2015
Phase I study of the anti-IGF1R antibody cixutumumab with everolimus and octreotide in advanced well-differentiated neuroendocrine tumors
Arvind Dasari, Alexandria Phan, Sanjay Gupta, et al.
American Journal of Medical Genetics. Part A
|
December 5, 2018
Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe
Ohad Wormser, Libe Gradstein, Einat Kadar, et al.
Journal of Medical Genetics
|
November 23, 2018
<i>SEC31A</i> mutation affects ER homeostasis, causing a neurological syndrome
Daniel Halperin, Rotem Kadir, Yonatan Perez, et al.
European Journal of Human Genetics : EJHG
|
May 11, 2017
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation
Yuval Yogev, Yonatan Perez, Iris Noyman, et al.
Page
of 6