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「"Leblanc T "[Author]」の検索結果

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Genotype/phenotype correlations of childhood-onset congenital sideroblastic anaemia in a European cohort.

Outcome of relapse in children and adolescents with B-cell non-Hodgkin lymphoma and mature acute leukemia: A report from the French LMB study.

Impact of cancer chemotherapy before ovarian cortex cryopreservation on ovarian tissue transplantation.

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.

Post-transplant outcome of ovarian tissue cryopreserved after chemotherapy in hematological malignancies.

Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1: Implications for disease severity.

Neurological Involvement in Childhood Evans Syndrome.

The effect of age in patients with acquired aplastic anaemia treated with immunosuppressive therapy: comparison of Adolescents and Young Adults with children and older adults.

Mutations in gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.

PROMIDISα: a TCRα signature associated with immunodeficiencies caused by V(D)J recombination defects.

Treatment with cyclosporin in auto-immune cytopenias in children: The experience from the French cohort OBS'CEREVANCE.

Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients.

Refining the phenotype associated with biallelic DNAJC21 mutations.

FDG-PET response of skeletal (bone marrow and bone) involvement after induction chemotherapy in pediatric Hodgkin lymphoma - Are specific response criteria required?

Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia.

Nationwide Survey on the Use of Horse Antithymocyte Globulins (ATGAM) in Patients with Acquired Aplastic Anemia: A Report on Behalf of the French Reference Center for Aplastic Anemia.

Iron Chelation Resulting in Renal Phosphate Wasting.

The severe phenotype of Diamond-Blackfan anemia is modulated by heat shock protein 70.

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