Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 86

1.

Tremor Relief and Structural Integrity after MRI-guided Focused US Thalamotomy in Tremor Disorders.

Zur G, Lesman-Segev OH, Schlesinger I, Goldsher D, Sinai A, Zaaroor M, Assaf Y, Eran A, Kahn I.

Radiology. 2020 Jan 7:191624. doi: 10.1148/radiol.2019191624. [Epub ahead of print]

PMID:
31909701
2.

Long-term effects of brief hypoxia due to cardiac arrest: Hippocampal reductions and memory deficits.

Stamenova V, Nicola R, Aharon-Peretz J, Goldsher D, Kapeliovich M, Gilboa A.

Resuscitation. 2018 May;126:65-71. doi: 10.1016/j.resuscitation.2018.02.016. Epub 2018 Feb 21.

PMID:
29474878
3.

Sequence variation in PPP1R13L results in a novel form of cardio-cutaneous syndrome.

Falik-Zaccai TC, Barsheshet Y, Mandel H, Segev M, Lorber A, Gelberg S, Kalfon L, Ben Haroush S, Shalata A, Gelernter-Yaniv L, Chaim S, Raviv Shay D, Khayat M, Werbner M, Levi I, Shoval Y, Tal G, Shalev S, Reuveni E, Avitan-Hersh E, Vlodavsky E, Appl-Sarid L, Goldsher D, Bergman R, Segal Z, Bitterman-Deutsch O, Avni O.

EMBO Mol Med. 2017 Sep;9(9):1326. doi: 10.15252/emmm.201708209. No abstract available.

4.

Magnetic resonance-guided focused ultrasound thalamotomy for tremor: a report of 30 Parkinson's disease and essential tremor cases.

Zaaroor M, Sinai A, Goldsher D, Eran A, Nassar M, Schlesinger I.

J Neurosurg. 2018 Jan;128(1):202-210. doi: 10.3171/2016.10.JNS16758. Epub 2017 Feb 24.

PMID:
28298022
5.

Sequence variation in PPP1R13L results in a novel form of cardio-cutaneous syndrome.

Falik-Zaccai TC, Barsheshet Y, Mandel H, Segev M, Lorber A, Gelberg S, Kalfon L, Ben Haroush S, Shalata A, Gelernter-Yaniv L, Chaim S, Raviv Shay D, Khayat M, Werbner M, Levi I, Shoval Y, Tal G, Shalev S, Reuveni E, Avitan-Hersh E, Vlodavsky E, Appl-Sarid L, Goldsher D, Bergman R, Segal Z, Bitterman-Deutsch O, Avni O.

EMBO Mol Med. 2017 Mar;9(3):319-336. doi: 10.15252/emmm.201606523. Erratum in: EMBO Mol Med. 2017 Sep;9(9):1326.

6.

Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria.

Mandel H, Saita S, Edvardson S, Jalas C, Shaag A, Goldsher D, Vlodavsky E, Langer T, Elpeleg O.

J Med Genet. 2016 Oct;53(10):690-6. doi: 10.1136/jmedgenet-2016-103922. Epub 2016 May 12.

PMID:
27208207
7.

Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.

Srour M, Hamdan FF, McKnight D, Davis E, Mandel H, Schwartzentruber J, Martin B, Patry L, Nassif C, Dionne-Laporte A, Ospina LH, Lemyre E, Massicotte C, Laframboise R, Maranda B, Labuda D, D├ęcarie JC, Rypens F, Goldsher D, Fallet-Bianco C, Soucy JF, Laberge AM, Maftei C; Care4Rare Canada Consortium, Boycott K, Brais B, Boucher RM, Rouleau GA, Katsanis N, Majewski J, Elpeleg O, Kukolich MK, Shalev S, Michaud JL.

Am J Hum Genet. 2015 Nov 5;97(5):744-53. doi: 10.1016/j.ajhg.2015.09.009. Epub 2015 Oct 17.

8.

MRI Guided Focused Ultrasound Thalamotomy for Moderate-to-Severe Tremor in Parkinson's Disease.

Schlesinger I, Eran A, Sinai A, Erikh I, Nassar M, Goldsher D, Zaaroor M.

Parkinsons Dis. 2015;2015:219149. doi: 10.1155/2015/219149. Epub 2015 Sep 2.

9.

Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Magen D, Ofir A, Berger L, Goldsher D, Eran A, Katib N, Nijem Y, Vlodavsky E, Tzur S, Behar DM, Fellig Y, Mandel H.

Hum Genet. 2015 Mar;134(3):315. doi: 10.1007/s00439-015-1530-0. No abstract available.

PMID:
25609191
10.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Magen D, Ofir A, Berger L, Goldsher D, Eran A, Katib N, Nijem Y, Vlodavsky E, Tzur S, Behar DM, Fellig Y, Mandel H.

Hum Genet. 2015 Mar;134(3):305-14. doi: 10.1007/s00439-014-1522-5. Epub 2015 Jan 6. Erratum in: Hum Genet. 2015 Mar;134(3):315. Katib, Nassser [corrected to Katib, Nasser]; Zur, Shay [corrected to Tzur, Shay].

PMID:
25560765
11.

A deep penetrating facial congenital melanocytic tumor with bone involvement and ipsilateral eye blindness.

Bergman R, Ben-Arush MW, Bar-Shalom R, Gilboa M, Simon E, Hershkovitz D, Sabo E, Maly A, Gerami P, Goldsher D.

Am J Dermatopathol. 2015 Jan;37(1):e5-e11. doi: 10.1097/DAD.0000000000000048.

PMID:
25222197
12.

Delineation of C12orf65-related phenotypes: a genotype-phenotype relationship.

Spiegel R, Mandel H, Saada A, Lerer I, Burger A, Shaag A, Shalev SA, Jabaly-Habib H, Goldsher D, Gomori JM, Lossos A, Elpeleg O, Meiner V.

Eur J Hum Genet. 2014 Aug;22(8):1019-25. doi: 10.1038/ejhg.2013.284. Epub 2014 Jan 15.

13.

Clinical and imaging findings in patients with neurosyphilis: a study of a cohort and review of the literature.

Khamaysi Z, Bergman R, Telman G, Goldsher D.

Int J Dermatol. 2014 Jul;53(7):812-9. doi: 10.1111/ijd.12095. Epub 2013 Nov 21. Review.

PMID:
24261864
14.

Goldenhar syndrome and medulloblastoma: a coincidental association? The first case report.

Aizenbud D, Shoham NV, Constantini S, Nevo N, Ben Arush M, Raz M, Rachmiel A, Goldsher D.

J Craniomaxillofac Surg. 2014 Jul;42(5):e91-6. doi: 10.1016/j.jcms.2013.07.003. Epub 2013 Aug 13.

PMID:
23953647
15.

Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1.

Sarig O, Goldsher D, Nousbeck J, Fuchs-Telem D, Cohen-Katsenelson K, Iancu TC, Manov I, Saada A, Sprecher E, Mandel H.

Am J Med Genet A. 2013 Sep;161A(9):2204-15. doi: 10.1002/ajmg.a.36059. Epub 2013 Aug 5.

PMID:
23918762
16.

Subependymal mass lesions and peripheral polyneuropathy in adult-onset glutaric aciduria type I.

Herskovitz M, Goldsher D, Sela BA, Mandel H.

Neurology. 2013 Aug 27;81(9):849-50. doi: 10.1212/WNL.0b013e3182a2cbf2. Epub 2013 Jul 24.

PMID:
23884036
17.

Craniofacial magnetic resonance imaging with a gold solder-filled chain-like wire fixed orthodontic retainer.

Aizenbud D, Hazan-Molina H, Einy S, Goldsher D.

J Craniofac Surg. 2012 Nov;23(6):e654-7. doi: 10.1097/SCS.0b013e3182710609.

PMID:
23172516
18.

Ischemic stroke due to a calcified embolus from the mitral annular valve.

Herskovitz M, Telman G, Carasso S, Symonovitz A, Goldsher D.

Neurology. 2012 Mar 20;78(12):931. doi: 10.1212/WNL.0b013e31824c46f5. No abstract available.

PMID:
22431740
19.

A prospective evaluation of a protocol for magnetic resonance imaging of patients with implanted cardiac devices.

Nazarian S, Hansford R, Roguin A, Goldsher D, Zviman MM, Lardo AC, Caffo BS, Frick KD, Kraut MA, Kamel IR, Calkins H, Berger RD, Bluemke DA, Halperin HR.

Ann Intern Med. 2011 Oct 4;155(7):415-24. doi: 10.7326/0003-4819-155-7-201110040-00004.

20.

CEDNIK syndrome results from loss-of-function mutations in SNAP29.

Fuchs-Telem D, Stewart H, Rapaport D, Nousbeck J, Gat A, Gini M, Lugassy Y, Emmert S, Eckl K, Hennies HC, Sarig O, Goldsher D, Meilik B, Ishida-Yamamoto A, Horowitz M, Sprecher E.

Br J Dermatol. 2011 Mar;164(3):610-6. doi: 10.1111/j.1365-2133.2010.10133.x. Epub 2011 Feb 17.

PMID:
21073448

Supplemental Content

Loading ...
Support Center