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Acontinuación brindamos Bibliografía con sus correspondientes links de acceso para que puedan ser consultados de manera completa:

J Thromb Haemost. 2020 Oct;18(10):2486-2495. doi: 10.1111/jth.15006. Epub 2020 Sep 11

ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura

X Long Zheng 1 , Sara K Vesely 2 , Spero R Cataland 3 , Paul Coppo 4 ,Brian Geldziler 5 , Alfonso Iorio 6 7 , Masanori Matsumoto 8 , Reem A Mustafa 9 , Menaka Pai 7 , Gail Rock 10 , Lene Russell 11 , Rawan Tarawneh 12 ,Julie Valdes 13 ,Flora Peyvandi 1415

J Clin Med. 2021 Feb 2;10(3):536. doi: 10.3390/jcm10030536.

Thrombotic Thrombocytopenic Purpura: Pathophysiology, Diagnosis, and Management

Senthil Sukumar 1 , Bernhard Lämmle 2 3 4 , Spero R Cataland 1

Blood Res.2019 Sep; 54(3): 218 228.Published online 2019 Sep 25. doi:10.5045/br.2019.54.3.218

Prognostic utility of ADAMTS13 activity for the atypical hemolytic uremic syndrome (aHUS) and comparison of complement serology between aHUS and thrombotic thrombocytopenic purpura

Jisu Oh, 1 Doyeun Oh , 1 Seon Ju Lee , 2 Jeong Oh Kim , 2 Nam Keun Kim, 2 So Young Chong, 1 Ji Young Huh, 3 Ross I. Baker, 4

Br J Haematol.2019 Aug;186(3):490-498.doi: 10.1111/bjh.15932.Epub 2019 May 26.

Utilizing a PLASMIC score-based approach in the management of suspected immune thrombotic thrombocytopenic purpura: a cost minimization analysis within the Harvard TMA Research Collaborative

Vivek A Upadhyay 1 2 , Benjamin P Geisler  1 2 ,  Lova Sun  1 2 , Lynne Uhl  2 3 , Richard M Kaufman  2 4 , Christopher Stowell  2 5 , Robert S Makar  2 5 , Pavan K Bendapudi  2 5 6 7

Int J Lab Hematol. 2022 Sep; 44(Suppl 1): 101–113.Published online 2022 Sep 8. doi: 10.1111/ijlh.13954

Diagnosis and treatment of thrombotic microangiopathy

Gemma L. Thompson  1 , 2  and David Kavanagh  1 , 2

Can J Kidney Health Dis. 2021 Apr 22;8:20543581211008707. doi: 10.1177/20543581211008707.

Making the Correct Diagnosis in Thrombotic Microangiopathy: A Narrative Review

Philip A. McFarlane, 1  Martin Bitzan, 2,3  Catherine Broome, 4  Dana Baran, 5  Jocelyn Garland, 6  Louis-Philippe Girard, 7   Kuljit Grewal , 8  Anne-Laure Lapeyraque, 9  Christopher Jordan Patriquin, 10  Katerina Pavenski, 11  and Christoph Licht 12

Res Pract Thromb Haemost. 2022 Mar; 6(3): e12708.

Thrombotic microangiopathies: An illustrated review

Mouhamed Yazan Abou‐Ismail, MD,  1  Sargam Kapoor , MD,  2  Divyaswathi Citla Sridhar , MD,  3  Lalitha Nayak , MD,  4  and Sanjay Ahuja, MD, MSc  5

Clin J Am Soc Nephrol. 2021 Jun;16(6):942-956. doi: 10.2215/CJN.11830720.

Inherited Kidney Complement Diseases

Mathieu Lemaire,  1 , 2 , 3  Damien Noone ,  1 , 3  Anne-Laure Lapeyraque ,  4 , 5  Christoph Licht ,  1 , 2, 3  and Véronique Frémeaux-Bacchi  6

Clin Kidney J. 2021 Apr; 14(4): 1055–1066.

Thrombotic microangiopathies assessment: mind the complement

Miquel Blasco, 1,2  Elena Guillén, 1  Luis F Quintana, 1,2  Adriana Garcia-Herrera, 3  GastónPiñeiro, 1,2  Esteban Poch, 1,2   Enric Carreras , 4,5  Josep M Campistol, 1,2  Maribel Diaz-Ricart, 5,6  and Marta Palomo 4,5,6

Am J Hematol . 2023 May:98 Suppl 4:S44-S56.  doi: 10.1002/ajh.26854.

Complement-driven hemolytic uremic syndrome

Juliette Leon  1 2 3 4 , Marie-Bénédicte LeStang  1 4 , Rebecca Sberro-Soussan  1 4 , Aude Servais  1 4 ,  Dany Anglicheau  1 2 4 , Véronique Frémeaux-Bacchi  5 ,  Julien Zuber  1 2 3 4