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Refinado por: Base de dados/Biblioteca: Oxford University Press:Jisc Collections:Medicine Collection:2018 remover
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1
Congenital myopathy is caused by mutation of HACD1
Congenital myopathy is caused by mutation of HACD1
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Congenital myopathy is caused by mutation of HACD1

Muhammad, Emad ; Reish, Orit ; Ohno, Yusuke ; Scheetz, Todd ; Deluca, Adam ; Searby, Charles ; Regev, Miriam ; Benyamini, Lilach ; Fellig, Yakov ; Kihara, Akio ; Sheffield, Val C ; Parvari, Ruti

Human molecular genetics, 2013-12, Vol.22 (25), p.5229-5236 [Periódico revisado por pares]

England: Oxford University Press

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2
Pax7, Pax3 and Mamstr genes are involved in skeletal muscle impaired regeneration of dy2J/dy2J mouse model of Lama2-CMD
Pax7, Pax3 and Mamstr genes are involved in skeletal muscle impaired regeneration of dy2J/dy2J mouse model of Lama2-CMD
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Pax7, Pax3 and Mamstr genes are involved in skeletal muscle impaired regeneration of dy2J/dy2J mouse model of Lama2-CMD

Yanay, Nurit ; Elbaz, Moran ; Konikov-Rozenman, Jenya ; Elgavish, Sharona ; Nevo, Yuval ; Fellig, Yakov ; Rabie, Malcolm ; Mitrani-Rosenbaum, Stella ; Nevo, Yoram

Human molecular genetics, 2019-10, Vol.28 (20), p.3369-3390 [Periódico revisado por pares]

England

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3
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder
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Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder

Lossos, Alexander ; Elazar, Nimrod ; Lerer, Israela ; Schueler-Furman, Ora ; Fellig, Yakov ; Glick, Benjamin ; Zimmerman, Bat-El ; Azulay, Haim ; Dotan, Shlomo ; Goldberg, Sharon ; Gomori, John M ; Ponger, Penina ; Newman, J P ; Marreed, Hodaifah ; Steck, Andreas J ; Schaeren-Wiemers, Nicole ; Mor, Nofar ; Harel, Michal ; Geiger, Tamar ; Eshed-Eisenbach, Yael ; Meiner, Vardiella ; Peles, Elior

Brain (London, England : 1878), 2015-09, Vol.138 (Pt 9), p.2521-2536 [Periódico revisado por pares]

England: Oxford University Press

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4
MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12
MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12
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MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12

Lossos, Alexander ; Oldfors, Anders ; Fellig, Yakov ; Meiner, Vardiella ; Argov, Zohar ; Tajsharghi, Homa

Brain (London, England : 1878), 2013-07, Vol.136 (Pt 7), p.e238-e238 [Periódico revisado por pares]

England

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5
PATH-10. MicroRNAs AS PREDICTORS FOR CNS RELAPSE OF SYSTEMIC DIFFUSE LARGE B-CELL LYMPHOMA
PATH-10. MicroRNAs AS PREDICTORS FOR CNS RELAPSE OF SYSTEMIC DIFFUSE LARGE B-CELL LYMPHOMA
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PATH-10. MicroRNAs AS PREDICTORS FOR CNS RELAPSE OF SYSTEMIC DIFFUSE LARGE B-CELL LYMPHOMA

Pillar, Nir ; Bairey, Osnat ; Goldschmidt, Neta ; Fellig, Yakov ; Rosenblat, Yevgenia ; Shehtman, Itchak ; Haguel, Danielle ; Raanani, Pia ; Siegal, Tali

Neuro-oncology (Charlottesville, Va.), 2017-11, Vol.19 (suppl_6), p.vi172-vi172 [Periódico revisado por pares]

US: Oxford University Press

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6
CSIG-13. ANDROGEN RECEPTOR IS INVOLVED IN GLIOBLASTOMA AND PRESENTS A POTENTIAL THERAPEUTIC TARGET
CSIG-13. ANDROGEN RECEPTOR IS INVOLVED IN GLIOBLASTOMA AND PRESENTS A POTENTIAL THERAPEUTIC TARGET
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CSIG-13. ANDROGEN RECEPTOR IS INVOLVED IN GLIOBLASTOMA AND PRESENTS A POTENTIAL THERAPEUTIC TARGET

Lavon, Iris ; Zalsman, Nomi ; Canello, Tamar ; Charbit, Hanna ; Zelikovitch, Bracha ; Mordechai, Anat ; Fellig, Yakov ; Rabani, Stav ; Shahar, Tal ; Lossos, Alexander

Neuro-oncology (Charlottesville, Va.), 2016-11, Vol.18 (suppl_6), p.vi43-vi43 [Periódico revisado por pares]

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7
CSIG-24. ANDROGEN RECEPTOR IS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA
CSIG-24. ANDROGEN RECEPTOR IS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA
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CSIG-24. ANDROGEN RECEPTOR IS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA

Zalsman, Nomi ; Canello, Tamar ; Ovadia, Haim ; Charbit, Hanna ; Zelikovitch, Bracha ; Mordechai, Anat ; Fellig, Yakov ; Rabani, Stav ; Shahar, Tal ; Lossos, Alexander ; Lavon, Iris

Neuro-oncology (Charlottesville, Va.), 2017-11, Vol.19 (suppl_6), p.vi54-vi55 [Periódico revisado por pares]

US: Oxford University Press

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8
NIMG-52. RADIATION-INDUCED VASCULAR MALFORMATIONS MIMICKING TUMOR IN MRI-BASED TREATMENT RESPONSE ASSESSMENT MAPS (TRAMs)
NIMG-52. RADIATION-INDUCED VASCULAR MALFORMATIONS MIMICKING TUMOR IN MRI-BASED TREATMENT RESPONSE ASSESSMENT MAPS (TRAMs)
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NIMG-52. RADIATION-INDUCED VASCULAR MALFORMATIONS MIMICKING TUMOR IN MRI-BASED TREATMENT RESPONSE ASSESSMENT MAPS (TRAMs)

Zach, Leor ; Guez, David ; Last, David ; Daniels, Dianne ; Sharabi, Shirley ; Nass, Dvora ; Nissim, Ouzi ; Spiegelmann, Roberto ; Tsarfaty, Galia ; Hoffmann, Chen ; Talianski, Alisa ; Shoshan, Yigal ; Fellig, Yakov ; Harnof, Sagi ; Cohen, Zvi ; Mardor, Yael

Neuro-oncology (Charlottesville, Va.), 2017-11, Vol.19 (suppl_6), p.vi153-vi154 [Periódico revisado por pares]

US: Oxford University Press

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9
MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12: Correspondence
MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12: Correspondence
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MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12: Correspondence

Lossos, Alexander ; Oldfors, Anders ; Fellig, Yakov ; Meiner, Vardiella ; Argov, Zohar ; Tajsharghi, Homa

Brain (London, England : 1878), 2013, Vol.136 (Pt 7) [Periódico revisado por pares]

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