Lanfranchi A - Search Results

1

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: lanfranchi a. Immunodeficiency. 1993;4(1-4):271-6. Immunodeficiency. 1993. PMID: 8167717 No abstract available.

2

Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

Notarangelo LD, Parolini O, Porta F, Locatelli F, Lanfranchi A, Marconi M, Nespoli L, Albertini A, Craig IW, Ugazio AG. Notarangelo LD, et al. Among authors: lanfranchi a. Hum Genet. 1991 Dec;88(2):237-41. doi: 10.1007/BF00206081. Hum Genet. 1991. PMID: 1684569

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: lanfranchi a. DNA Cell Biol. 1993 Sep;12(7):645-9. doi: 10.1089/dna.1993.12.645. DNA Cell Biol. 1993. PMID: 8397823

4

In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI).

Wengler GS, Lanfranchi A, Frusca T, Verardi R, Neva A, Brugnoni D, Giliani S, Fiorini M, Mella P, Guandalini F, Mazzolari E, Pecorelli S, Notarangelo LD, Porta F, Ugazio AG. Wengler GS, et al. Among authors: lanfranchi a. Lancet. 1996 Nov 30;348(9040):1484-7. doi: 10.1016/s0140-6736(96)09392-0. Lancet. 1996. PMID: 8942778

5

Single-center analysis of long-term outcome after hematopoietic cell transplantation in children with congenital severe T cell immunodeficiency.

Mazzolari E, de Martiis D, Forino C, Lanfranchi A, Giliani S, Marzollo R, Airò P, Imberti L, Porta F, Notarangelo LD. Mazzolari E, et al. Among authors: lanfranchi a. Immunol Res. 2009;44(1-3):4-17. doi: 10.1007/s12026-008-8022-4. Immunol Res. 2009. PMID: 18592143

6

Reconstitution of T-cell compartment after in utero stem cell transplantation: analysis of T-cell repertoire and thymic output.

Pirovano S, Notarangelo LD, Malacarne F, Mazzolari E, Porta F, Lanfranchi A, Giliani S, Zucca S, Pecorelli S, Albertini A, Ugazio AG, Imberti L. Pirovano S, et al. Among authors: lanfranchi a. Haematologica. 2004 Apr;89(4):450-61. Haematologica. 2004. PMID: 15075079

7

Functional depletion of T cells by vincristine and methylprednisolone as an in vitro model for the prevention of graft versus host disease.

Lanfranchi A, Andolina M, Tettoni K, Porta F, Locatelli F, De Manzini A, Candotti F, Albertini A. Lanfranchi A, et al. Haematologica. 1992 Jan-Feb;77(1):11-5. Haematologica. 1992. PMID: 1398275

8

The reconstitution of cellular immunity after bone marrow transplantation in children.

Lanfranchi A, Porta F, Locatelli F, Zecca M, Nespoli L, Albertini A. Lanfranchi A, et al. Haematologica. 1992 Jul-Aug;77(4):336-47. Haematologica. 1992. PMID: 1427444 Review. No abstract available.

9

[Cellular and molecular therapy in severe combined immunodeficiencies].

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

10

[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: lanfranchi a. Pediatr Med Chir. 1991 Jan-Feb;13(1):27-30. Pediatr Med Chir. 1991. PMID: 2052452 Italian.

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