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Your search keyword '"Maria Teresa Romano"' showing total 14 results

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1. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome

2. Abstracts from the 50th European Society of Human Genetics Conference: Oral Presentations

3. An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction

4. Variant

5. Variant PADI3 in Central Centrifugal Cicatricial Alopecia

6. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex

7. Congenital Anonychia and Uncombable Hair Syndrome:Coinheritance of Homozygous Mutations in RSPO4 and PADI3

8. Two Different Platelet Thresholds for Bleeding Prophylaxis in Children with Malignancies or Non-Malignant Disorders: The Bambino Gesù Children's Hospital Experience

9. 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia

10. Extracorporeal photopheresis for paediatric patients experiencing graft-versus-host disease (GVHD)

11. HLA-Haploidentical TCR αβ/CD19-Depleted Hematopoietic Stem Cell Transplantation in Children with Fanconi Anemia

12. An unusual case of anisocoria by vegetal intoxication: a case report

13. Immune Reconstitution after Adoptive Infusion of BPX501 Cells (donor T cells transduced with iC9 suicide gene) in Children Given Alpha/Beta T-Cell Depleted HLA-Haploidentical Hematopoietic Stem Cell Transplantation (haplo-HSCT): Preliminary Phenotypic and Functional Results of a Phase I-II Trial

14. Children with Acute Leukemia Given Hematopoietic Stem Cell Transplantation (HSCT) from an HLA-Compatible Sibling, or an Unrelated Donor (UD) or an HLA-Haploidentical Relative after Alpha/Beta T-Cell Depletion Have a Comparable Outcome

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