Notarangelo LD - Search Results

1

Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1).

Wengler GS, Giliani S, Fiorini M, Mella P, Mantuano E, Zanola A, Pollonini G, Eibl MM, Ugazio AG, Notarangelo LD, Parolini O. Wengler GS, et al. Among authors: notarangelo ld. Br J Haematol. 1998 Jun;101(3):586-91. doi: 10.1046/j.1365-2141.1998.00721.x. Br J Haematol. 1998. PMID: 9633906 Free article.

2

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

Maestrini E, Rivella S, Tribioli C, Rocchi M, Camerino G, Santachiara-Benerecetti S, Parolini O, Notarangelo LD, Toniolo D. Maestrini E, et al. Among authors: notarangelo ld. Am J Hum Genet. 1992 Jan;50(1):156-63. Am J Hum Genet. 1992. PMID: 1346076 Free PMC article.

3

Carrier detection in X-linked adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis.

Notarangelo LD, Parolini O, Baiguini G, Buzi F, Paterlini C, Perini A, Rimoldi M, Tiberti S, Uziel G, Notarangelo L, et al. Notarangelo LD, et al. Among authors: notarangelo l. Eur J Pediatr. 1992 Oct;151(10):761-3. doi: 10.1007/BF01959086. Eur J Pediatr. 1992. PMID: 1425799

4

Insulin-dependent diabetes mellitus and severe atopic dermatitis in a child with adenosine deaminase deficiency.

Notarangelo LD, Stoppoloni G, Toraldo R, Mazzolari E, Coletta A, Airò P, Bordignon C, Ugazio AG. Notarangelo LD, et al. Eur J Pediatr. 1992 Nov;151(11):811-4. doi: 10.1007/BF01957930. Eur J Pediatr. 1992. PMID: 1468454

5

Immunodeficiency with hyper-IgM (HIM).

Notarangelo LD, Duse M, Ugazio AG. Notarangelo LD, et al. Immunodefic Rev. 1992;3(2):101-21. Immunodefic Rev. 1992. PMID: 1554497 Review.

6

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

7

Primary immunodeficiencies: milestones in the history of pediatric immunology.

Burgio GR, Notarangelo LD, Duse M, Ugazio AG. Burgio GR, et al. Among authors: notarangelo ld. Pediatr Hematol Oncol. 1991 Jul-Sep;8(3):203-14. doi: 10.3109/08880019109033453. Pediatr Hematol Oncol. 1991. PMID: 1742178 Review.

8

Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages.

Notarangelo LD, Parolini O, Albertini A, Duse M, Mazzolari E, Plebani A, Camerino G, Ugazio AG. Notarangelo LD, et al. Hum Genet. 1991 Dec;88(2):130-4. doi: 10.1007/BF00206059. Hum Genet. 1991. PMID: 1757090

9

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. Bone Marrow Transplant. 1991;7 Suppl 3:136-8. Bone Marrow Transplant. 1991. PMID: 1855078 No abstract available.

10

[Primary immunodeficiency 1991: new uses and prospects of genetic counseling].

Notarangelo LD, Parolini O, Lusardi M, Mazzolari E, Ugazio AG. Notarangelo LD, et al. Pediatr Med Chir. 1991 Mar-Apr;13(2):129-33. Pediatr Med Chir. 1991. PMID: 1896377 Review. Italian.

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