Item request has been placed!

Item request cannot be made.

Processing Request

نتائج البحث

Display Settings

النتائج لكل صفحة: 10

Sort By: Relevance

Filter

فلترة النتائج

إعادة تعيين خيارات الفبترة

Item request has been placed!

Item request cannot be made.

Processing Request

Academic Journal

Acute cerebellar ataxia in lupus.

Authors : Chattopadhyay, P¹; Dhua, D; Philips, CA

Source: Lupus. Dec2011, Vol. 20 Issue 12, p1312-1315. 4p. 2 Black and White Photographs.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosis.

Authors : Szmulewicz, David J.¹ (AUTHOR); Waterston, John A.² (AUTHOR); MacDougall, Hamish G.³ (AUTHOR)

Source: Annals of the New York Academy of Sciences. Sep2011, Vol. 1233 Issue 1, p139-147. 9p. 2 Color Photographs, 2 Graphs.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Clinical, electrophysiological, and MRI findings in patients with cerebellar ataxia and a bilaterally pathological head-impulse test.

Authors : Kirchner, Hanni¹ (AUTHOR); Kremmyda, Olympia¹ (AUTHOR); Hüfner, Katharina¹ (AUTHOR)

Source: Annals of the New York Academy of Sciences. Sep2011, Vol. 1233 Issue 1, p127-138. 12p. 1 Color Photograph, 3 Charts.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene.

Authors : Sevin, Caroline¹ ; Ferdinandusse, Sacha²; Waterham, Hans R.²

Source: Orphanet Journal of Rare Diseases. 2011, Vol. 6 Issue 1, p8-11. 4p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics.

Authors : Whaley, Nathaniel Robb^1,2; Fujioka, Shinsuke²; Wszolek, Zbigniew K.²

Source: Orphanet Journal of Rare Diseases. 2011, Vol. 6 Issue 1, p33-45. 13p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Respective implications of glutamate decarboxylase antibodies in stiff person syndrome and cerebellar ataxia.

Authors : Manto, Mario U.¹; Hampe, Christiane S.² ; Rogemond, Véronique^3,4

Source: Orphanet Journal of Rare Diseases. 2011, Vol. 6 Issue 1, p3-16. 4p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Epileptic Seizure Following IV Tramadol in a Patient with Mental Retardation and Cerebellar Ataxia.

Authors : Yarkan Uysal, Hale¹; Bilimgut, Bağnu¹; Dikmen, Bayazit¹

Source: Pain Medicine. May2011, Vol. 12 Issue 5, p833-836. 4p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Mycoplasma pneumonia'ya Bağlı Akut Serebellar Ataksi: İki Vaka Sunumu.

Authors : Hacifazlioğlu Eldeş, Nilüfer¹ ; Kuzdan, Canan²; Erbaş, Bahar¹

Source: Journal of the Child / Çocuk Dergisi. Dec2011, Vol. 11 Issue 4, p174-176. 3p. 1 Chart.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Cochlear implantation following cerebellar surgery.

Authors : Saeed, Shahad¹ (AUTHOR); Mawman, Deborah¹ (AUTHOR); Green, Kevin¹ (AUTHOR)

Source: Cochlear Implants International: An Interdisciplinary Journal. 2011, Vol. 12 Issue 3, p185-188. 4p.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

Academic Journal

Using interpretative phenomenological analysis to inform physiotherapy practice: An introduction with reference to the lived experience of cerebellar ataxia.

Authors : Cassidy, Elizabeth¹ (AUTHOR) ; Reynolds, Frances² (AUTHOR); Naylor, Sandra³ (AUTHOR)

Source: Physiotherapy Theory & Practice. May2011, Vol. 27 Issue 4, p263-277. 15p. 1 Chart.

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي

نتائج البحث

فلترة النتائج

Acute cerebellar ataxia in lupus.

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosis.

Clinical, electrophysiological, and MRI findings in patients with cerebellar ataxia and a bilaterally pathological head-impulse test.

Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene.

Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics.

Respective implications of glutamate decarboxylase antibodies in stiff person syndrome and cerebellar ataxia.

Epileptic Seizure Following IV Tramadol in a Patient with Mental Retardation and Cerebellar Ataxia.

Mycoplasma pneumonia'ya Bağlı Akut Serebellar Ataksi: İki Vaka Sunumu.

Cochlear implantation following cerebellar surgery.

Using interpretative phenomenological analysis to inform physiotherapy practice: An introduction with reference to the lived experience of cerebellar ataxia.

اتصل بنا

اتبع