Porta 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: porta 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. Pediatr Med Chir. 1991 Jan-Feb;13(1):27-30. Pediatr Med Chir. 1991. PMID: 2052452 Italian.

3

Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experience.

Mazzolari E, Moshous D, Forino C, De Martiis D, Offer C, Lanfranchi A, Giliani S, Imberti L, Pasic S, Ugazio AG, Porta F, Notarangelo LD. Mazzolari E, et al. Among authors: porta f. Bone Marrow Transplant. 2005 Jul;36(2):107-14. doi: 10.1038/sj.bmt.1705017. Bone Marrow Transplant. 2005. PMID: 15908971

4

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: porta f. Hum Genet. 1991 Dec;88(2):237-41. doi: 10.1007/BF00206081. Hum Genet. 1991. PMID: 1684569

5

[Cellular and molecular therapy in severe combined immunodeficiencies].

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

6

B cell function after haploidentical in utero bone marrow transplantation in a patient with severe combined immunodeficiency.

Bartolomé J, Porta F, Lafranchi A, Rodríguez-Molina JJ, Cela E, Cantalejo A, Fernández-Cruz E, Gómez-Pineda A, Ugazio AG, Notarangelo LD, Gil J. Bartolomé J, et al. Among authors: porta f. Bone Marrow Transplant. 2002 Apr;29(7):625-8. doi: 10.1038/sj.bmt.1703410. Bone Marrow Transplant. 2002. PMID: 11979315

7

Stem cell transplantation for primary immunodeficiencies.

Porta F, Forino C, De Martiis D, Soncini E, Notarangelo L, Tettoni K, D'Ippolito C, Soresina R, Shiha K, Berta S, Baffelli R, Bolda F, Bosi A, Schumacher FR, Lanfranchi A, Mazzolari E. Porta F, et al. Bone Marrow Transplant. 2008 Jun;41 Suppl 2:S83-6. doi: 10.1038/bmt.2008.61. Bone Marrow Transplant. 2008. PMID: 18545252

8

Immunological reconstitution after bone marrow transplantation.

Porta F, Mazzolari E, Lanfranchi A, Pennacchio M, Fischer A. Porta F, et al. Bone Marrow Transplant. 1996 Nov;18 Suppl 2:148-50. Bone Marrow Transplant. 1996. PMID: 8932818 Review. No abstract available.

9

Familial haemophagocytic lymphohistiocytosis treated with allogeneic bone marrow transplantation.

Nespoli L, Locatelli F, Bonetti F, Porta F, Zecca M, Gibardi A, Gambarana D, Vitale V, Burgio GR, Severi F. Nespoli L, et al. Among authors: porta f. Bone Marrow Transplant. 1991;7 Suppl 3:139-42. Bone Marrow Transplant. 1991. PMID: 1855079 No abstract available.

10

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

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