نتائج البحث

Lombardy diagnostic and therapeutic network of thrombotic microangiopathy

• Authors : I. Mancini; P. Agosti; M. Boscarino

Subjects: ADAMTS13; Differential diagnosis; Incidence

• Source: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)

تفاصيل العنوان

Lombardy diagnostic and therapeutic network of thrombotic microangiopathy.

• Authors : Mancini I; Agosti P ...

Subjects: ADAMTS13 Protein*/ADAMTS13 Protein*/ADAMTS13 Protein*/deficiency ; Purpura, Thrombotic Thrombocytopenic*/Purpura, Thrombotic Thrombocytopenic*/Purpura, Thrombotic Thrombocytopenic*/diagnosis ; Purpura, Thrombotic Thrombocytopenic*/Purpura, Thrombotic Thrombocytopenic*/Purpura, Thrombotic Thrombocytopenic*/epidemiology

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Jun 23; Vol. 17 (1), pp. 246. Date of Electronic Publication: 2022 Jun 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

Lessons learned from hemolytic uremic syndrome registries: recommendations for implementation

• Authors : Mina Lazem; Abbas Sheikhtaheri; Nakysa Hooman

Subjects: Registry; Hemolytic uremic syndrome; Thrombotic microangiopathy

• Source: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)

تفاصيل العنوان

Incidence of acquired thrombotic thrombocytopenic purpura in Germany: a hospital level study

• Authors : Wolfgang Miesbach; Jan Menne; Martin Bommer

Subjects: Epidemiology; Germany; Incidence

• Source: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)

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Real-world multidisciplinary outcomes of onasemnogene abeparvovec monotherapy in patients with spinal muscular atrophy type 1: experience of the French cohort in the first three years of treatment.

• Authors : Desguerre, Isabelle^1,2 (AUTHOR); Barrois, Rémi² (AUTHOR) ; Audic, Frédérique³ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 9/13/2024, Vol. 19 Issue 1, p1-11. 11p.

تفاصيل العنوان

Late-onset methylmalonic acidemia and homocysteinemia (cblC disease): systematic review.

• Authors : Arhip, Loredana^1,2 (AUTHOR) ; Brox-Torrecilla, Noemi³ (AUTHOR); Romero, Inmaculada⁴ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 1/20/2024, Vol. 19 Issue 1, p1-9. 9p.

تفاصيل العنوان

Combined methylmalonic acidemia and homocysteinemia presenting predominantly with late-onset diffuse lung disease: a case series of four patients

• Authors : Hui Xu; Jinrong Liu; Nan Zhou

Subjects: medicine.medical_specialty; Thrombotic microangiopathy; Methylmalonic acidemia

• Source: Orphanet Journal of Rare Diseases

تفاصيل العنوان

Incidence of acquired thrombotic thrombocytopenic purpura in Germany: a hospital level study.

• Authors : Miesbach, Wolfgang¹ (AUTHOR) ; Menne, Jan² (AUTHOR); Bommer, Martin³ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 11/15/2019, Vol. 14 Issue 1, p1-10. 10p.

تفاصيل العنوان

Atypical hemolytic uremic syndrome

• Authors : Chantal Loirat; Véronique Frémeaux-Bacchi

Subjects: Male; Hemolytic anemia; Atypical hemolytic uremic syndrome

• Source: Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 60 (2011)Orphanet Journal of Rare Diseases

تفاصيل العنوان

Lessons learned from hemolytic uremic syndrome registries: recommendations for implementation.

• Authors : Lazem, Mina¹ (AUTHOR); Sheikhtaheri, Abbas² (AUTHOR) ; Hooman, Nakysa³ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 5/25/2021, Vol. 16 Issue 1, p1-13. 13p.

تفاصيل العنوان