Notarangelo LD - Search Results

1

Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis.

Giliani S, Fiorini M, Mella P, Candotti F, Schumacher RF, Wengler GS, Lalatta F, Fasth A, Badolato R, Ugazio AG, Albertini A, Notarangelo LD. Giliani S, et al. Among authors: notarangelo ld. Prenat Diagn. 1999 Jan;19(1):36-40. Prenat Diagn. 1999. PMID: 10073904

2

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

de Saint Basile G, Notarangelo LD, Bonaiti-Pellié C, Doussau M, Prolini O, Craig IW, Ugazio A, Griscelli C, Fischer A. de Saint Basile G, et al. Among authors: notarangelo ld. Hum Genet. 1992 May;89(2):223-8. doi: 10.1007/BF00217127. Hum Genet. 1992. PMID: 1350264 Clinical Trial.

3

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

4

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.

5

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

6

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.

7

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

8

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.

9

[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.

10

Presentation of Wiskott Aldrich syndrome as isolated thrombocytopenia.

Notarangelo LD, Parolini O, Faustini R, Porteri V, Albertini A, Ugazio AG. Notarangelo LD, et al. Blood. 1991 Mar 1;77(5):1125-6. Blood. 1991. PMID: 1995098 Free article. No abstract available.

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