نتائج البحث

Systematic review of phenotypes in McLeod syndrome and case report of a progressive supranuclear palsy in a female carrier.

• Authors : Braun AA; Department of Neurology, University Hospital Zurich, Frauenklinikstrasse 26, 8091, Zurich, Switzerland. .; Jung HH

Subjects: Neuroacanthocytosis*/Neuroacanthocytosis*/Neuroacanthocytosis*/genetics ; Neuroacanthocytosis*/Neuroacanthocytosis*/Neuroacanthocytosis*/pathology ; Neuroacanthocytosis*/Neuroacanthocytosis*/Neuroacanthocytosis*/diagnosis Neuroacanthocytosis, Mcleod Type

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Aug 25; Vol. 19 (1), pp. 312. Date of Electronic Publication: 2024 Aug 25.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

Progressive Supranuclear palsy (PSP) disease progression, management, and healthcare resource utilization: a retrospective observational study in the US and Canada.

• Authors : Nysetvold E; AllStripes Research, San Francisco, California, USA.; Lopez LN

Subjects: Supranuclear Palsy, Progressive*/Supranuclear Palsy, Progressive*/Supranuclear Palsy, Progressive*/therapy ; Disease Progression*; Humans

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 May 23; Vol. 19 (1), pp. 215. Date of Electronic Publication: 2024 May 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

Innovative methodologies for rare diseases clinical trials.

• Authors : Nabbout, Rima^1,2,3 (AUTHOR) ; Hilgers, Ralf-Dieter⁴ (AUTHOR)

Subjects: *RARE diseases; *CLINICAL trials; *PROGRESSIVE supranuclear palsy

• Source: Orphanet Journal of Rare Diseases. 5/7/2024, Vol. 19 Issue 1, p1-2. 2p.

تفاصيل العنوان

An algorithm as a diagnostic tool for central ocular motor disorders, also to diagnose rare disorders.

• Authors : Kraus L; Department of Neurology and German Center for Vertigo and Balance Disorders, Ludwig-Maximilians University, Munich, Campus Grosshadern, Marchioninistr. 15, 81377, Munich, Germany. .; Kremmyda O

Subjects: Algorithms*; Rare Diseases/Rare Diseases/Rare Diseases/*diagnosis; Adult

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2019 Aug 08; Vol. 14 (1), pp. 193. Date of Electronic Publication: 2019 Aug 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

[Untitled]

Subjects: 0301 basic medicine; Wernicke Encephalopathy; business.industry

• Source: Orphanet Journal of Rare Diseases.

تفاصيل العنوان