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7 in total

Review 1. [Congenital dyserythropoietic anemias].

Authors: H Heimpel
Journal: Blut Date: 1975-11

2. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

Authors: Klaus Schwarz; Achille Iolascon; Fatima Verissimo; Nikolaus S Trede; Wyatt Horsley; Wen Chen; Barry H Paw; Karl-Peter Hopfner; Karlheinz Holzmann; Roberta Russo; Maria Rosaria Esposito; Daniela Spano; Luigia De Falco; Katja Heinrich; Brigitte Joggerst; Markus T Rojewski; Silverio Perrotta; Jonas Denecke; Ulrich Pannicke; Jean Delaunay; Rainer Pepperkok; Hermann Heimpel
Journal: Nat Genet Date: 2009-06-28 Impact factor: 38.330

3. Congenital dyserythropoietic anemia, type II (Hempas). First five reported cases in Italy.

Authors: T Barbui; M Cazzavillan; T Chisesi; R Battista; G Cartei; E Dini
Journal: Blut Date: 1974-12

4. Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria.

Authors: W F Rosse; G L Logue; J Adams; J H Crookston
Journal: J Clin Invest Date: 1974-01 Impact factor: 14.808

Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test).

Review 1. [Congenital dyserythropoietic anemias].

2. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

3. Congenital dyserythropoietic anemia, type II (Hempas). First five reported cases in Italy.

4. Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria.

5. Cell membrane receptors for serological reagents.

6. [Ultrastructure of erythroid cells in a case of congenital dyserythropoietic anaemia type II (author's transl)].

7. Congenital dyserythropoietic anaemia type II (HEMPAS): a family study.