نتائج البحث

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

• Authors : Braun, Andreas Albert¹ (AUTHOR) ; Jung, Hans Heinrich¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 8/25/2024, Vol. 19 Issue 1, p1-7. 7p.

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

• Authors : Nysetvold, Ella¹ (AUTHOR); Lopez, Lauren N.¹ (AUTHOR); Cogell, Ashley N.¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 5/23/2024, Vol. 19 Issue 1, p1-14. 14p.

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

• Authors : Andreas Albert Braun; Hans Heinrich Jung

Subjects: Progressive supranuclear palsy; McLeod syndrome; Neuroacanthocytosis

• Source: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-7 (2024)

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

• Authors : Ella Nysetvold; Lauren N. Lopez; Ashley N. Cogell

Subjects: Progressive supranuclear palsy; PSP; Real-world data

• Source: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-14 (2024)

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Innovative methodologies for rare diseases clinical trials.

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

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

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

• Authors : Kraus, Ludwig; Kremmyda, Olympia; Bremova-Ertl, Tatiana

Subjects: Adult; Male; Niemann-Pick Diseases

• Source: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)Kraus, Ludwig; Kremmyda, Olympia; Brémovà-Ertl, Tatiana; Barceló, Sebastià; Feil, Katharina;

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