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The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA. Chonat S, et al. Among authors: hsieh l. Front Physiol. 2019 Jul 3;10:815. doi: 10.3389/fphys.2019.00815. eCollection 2019. Front Physiol. 2019. PMID: 31333484 Free PMC article.
Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA. Chonat S, et al. Among authors: hsieh l. Front Physiol. 2019 Oct 18;10:1331. doi: 10.3389/fphys.2019.01331. eCollection 2019. Front Physiol. 2019. PMID: 31736770 Free PMC article.
MDS and MIRAGE.
Buchbinder D, Hsieh L, Frediani J, Zadeh N, Nael A. Buchbinder D, et al. Among authors: hsieh l. J Pediatr Hematol Oncol. 2022 Oct 1;44(7):421-422. doi: 10.1097/MPH.0000000000002540. Epub 2022 Aug 30. J Pediatr Hematol Oncol. 2022. PMID: 36044305 No abstract available.
Rare factor deficiencies.
Hsieh L, Nugent D. Hsieh L, et al. Curr Opin Hematol. 2012 Sep;19(5):380-4. doi: 10.1097/MOH.0b013e328356edd5. Curr Opin Hematol. 2012. PMID: 22872158 Review.
689 results