Candotti F - Search Results

1

Use of the highly polymorphic DNA marker CRI-S232 for monitoring of engraftment and chimerism following bone marrow transplantation.

Notarangelo LD, Parolini O, Porta F, Arrighini A, Basagni G, Candotti F, Cavagna A, Cossandi G, Crescini C, Faustini R, et al. Notarangelo LD, et al. Among authors: candotti f. Bone Marrow Transplant. 1991;7 Suppl 3:136-8. Bone Marrow Transplant. 1991. PMID: 1855078 No abstract available.

2

[Bone marrow transplantation in congenital defects of immunity].

Porta F, Notarangelo LD, Candotti F, Mazzolari E, Lanfranchi A, Ugazio AG. Porta F, et al. Among authors: candotti f. Pediatr Med Chir. 1991 Jan-Feb;13(1):27-30. Pediatr Med Chir. 1991. PMID: 2052452 Italian.

3

Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS).

Notarangelo LD, Candotti F, Parolini O, Mantuano E, Giliani S, Lanfranchi A, Albertini A. Notarangelo LD, et al. Among authors: candotti f. DNA Cell Biol. 1993 Sep;12(7):645-9. doi: 10.1089/dna.1993.12.645. DNA Cell Biol. 1993. PMID: 8397823

4

[Cellular and molecular therapy in severe combined immunodeficiencies].

Porta F, Candotti F, Arrighini A, Lanfranchi A, Ugazio AG. Porta F, et al. Among authors: candotti f. Pediatr Med Chir. 1991 Mar-Apr;13(2):135-8. Pediatr Med Chir. 1991. PMID: 1896378 Italian.

5

Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment.

Bozzi F, Lefranc G, Villa A, Badolato R, Schumacher RF, Khalil G, Loiselet J, Bresciani S, O'Shea JJ, Vezzoni P, Notarangelo LD, Candotti F. Bozzi F, et al. Among authors: candotti f. Br J Haematol. 1998 Sep;102(5):1363-6. doi: 10.1111/j.1365-2141.1998.tb08990.x. Br J Haematol. 1998. PMID: 9753072 Free article.

6

Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unit.

Mantuano E, Candotti F, Giliani S, Parolini O, Lusardi M, Zucchi M, Lanfranchi A, Porta F, Airò P, Albertini A, et al. Mantuano E, et al. Among authors: candotti f. Immunodeficiency. 1993;4(1-4):271-6. Immunodeficiency. 1993. PMID: 8167717 No abstract available.

7

Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a model.

Notarangelo LD, Giliani S, Mella P, Schumacher RF, Mazza C, Savoldi G, Rodriguez-Pérez C, Badolato R, Mazzolari E, Porta F, Candotti F, Ugazio AG. Notarangelo LD, et al. Among authors: candotti f. Immunobiology. 2000 Aug;202(2):106-19. doi: 10.1016/s0171-2985(00)80058-3. Immunobiology. 2000. PMID: 10993286 Review.

8

Serum soluble interleukin-2 receptor (IL-2R) in children with allergic disorders.

Guarnaccia S, Kurman CC, Notarangelo LD, La Grutta S, Candotti F, Ugazio AG, Nelson DL, Bellanti JA. Guarnaccia S, et al. Among authors: candotti f. Ann Allergy. 1993 Sep;71(3):259-62. Ann Allergy. 1993. PMID: 8373000 No abstract available.

9

Prenatal diagnosis of JAK3 deficient SCID.

Schumacher RF, Mella P, Lalatta F, Fiorini M, Giliani S, Villa A, Candotti F, Notarangelo LD. Schumacher RF, et al. Among authors: candotti f. Prenat Diagn. 1999 Jul;19(7):653-6. Prenat Diagn. 1999. PMID: 10419614

10

Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism.

Schumacher RF, Mella P, Badolato R, Fiorini M, Savoldi G, Giliani S, Villa A, Candotti F, Tampalini A, O'Shea JJ, Notarangelo LD. Schumacher RF, et al. Among authors: candotti f. Hum Genet. 2000 Jan;106(1):73-9. doi: 10.1007/s004390051012. Hum Genet. 2000. PMID: 10982185

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