E-LIB Suche - Ergebnisse für: Da Costa, Lydie - Sprache DE

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1

Acute fetal leukemia: When should it be suspected? What ass..:

Forey, Pierre‐Louis ; Favier, Maud ; Beneteau, Claire...
Prenatal Diagnosis. , 2024

Link: https://doi.org/10.1002/..

2

Lentivirus-mediated gene therapy corrects ribosomal biogene..:

Giménez, Yari ; Palacios, Manuel ; Sánchez-Domínguez, Rebeca...
JCI Insight. 9 (2024) 10 - p. , 2024

Link: https://doi.org/10.1172/..

3

Next generation sequencing (NGS) interest in deciphering er..:

Allegrini, Benoit ; NGuyen, Ludivine David ; Mignotet, Morgane...
Blood Cells, Molecules, and Diseases. 103 (2023) - p. 102780 , 2023

Link: https://doi.org/10.1016/..

4

Relevance of Howell‐Jolly body counts for measuring spleen ..:

Pourdieu, Charlotte ; El Hoss, Sara ; Le Roux, Enora...
American Journal of Hematology. 98 (2023) 5 - p. , 2023

Link: https://doi.org/10.1002/..

5

GATA-1 Defects in Diamond–Blackfan Anemia: Phenotypic Chara..:

van Dooijeweert, Birgit ; Kia, Sima Kheradmand ; Dahl, Niklas...
Genes. 13 (2022) 3 - p. 447 , 2022

Link: https://doi.org/10.3390/..

6

The use of next‐generation sequencing in the diagnosis of r..:

Roy, Noémi B. A. ; Da Costa, Lydie ; Russo, Roberta...
British Journal of Haematology. 198 (2022) 3 - p. 459-477 , 2022

Link: https://doi.org/10.1111/..

7

Agranulocytosis in patients with Diamond‐Blackfan anaemia (..:

Lecornec, Nicolas ; Castex, Marie‐Pierre ; Réguerre, Yves...
British Journal of Haematology. 199 (2022) 2 - p. 285-288 , 2022

Link: https://doi.org/10.1111/..

8

HEATR3 variants impair nuclear import of uL18 (RPL5) and dr..:

O'Donohue, Marie-Françoise ; Da Costa, Lydie ; Lezzerini, Marco...
Blood. 139 (2022) 21 - p. 3111-3126 , 2022

Link: https://doi.org/10.1182/..

9

Unexplained iron overload with haemolytic anaemia should pr..:

Rieu, Jean‐Baptiste ; Largeaud, Laetitia ; Da Costa, Lydie.
British Journal of Haematology. 197 (2022) 2 - p. 132-132 , 2022

Link: https://doi.org/10.1111/..

10

Hereditary spherocytosis associated with Noonan syndrome mi..:

Faggetter, Sarah ; Ferster, Alina ; Dedeken, Laurence...
Pediatric Blood & Cancer. 70 (2022) 4 - p. , 2022

Link: https://doi.org/10.1002/..

11

Retinal atrophy and markers of systemic and cerebrovascular..:

Martin, Gilles C. ; Brousse, Valentine ; Connes, Philippe...
European Journal of Ophthalmology. 32 (2022) 6 - p. 3258-3266 , 2022

Link: https://doi.org/10.1177/..

12

The Use of Next-generation Sequencing in the Diagnosis of R..:

Roy, Noémi B. A. ; Da Costa, Lydie ; Russo, Roberta...
HemaSphere. 6 (2022) 6 - p. e739 , 2022

Link: https://doi.org/10.1097/..

13

Brain injury pathophysiology study by a multimodal approach..:

Brousse, Valentine ; Pondarre, Corinne ; Kossorotoff, Manoelle...
Haematologica. 107 (2021) 4 - p. 958-965 , 2021

Link: https://doi.org/10.3324/..

14

Biallelic mutations in the SARS2 gene presenting as congeni..:

Colin, Elia ; Courtois, Geneviève ; Brouzes, Chantal...
Haematologica. 106 (2021) 12 - p. 3202-3205 , 2021

Link: https://doi.org/10.3324/..

15

The Glucocorticoid Receptor Polymorphism Landscape in Patie..:

Lonetti, Annalisa ; Indio, Valentina ; Dianzani, Irma...
Frontiers in Physiology. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

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