Stuppia L - Search Results

1

Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome.

Brancati F, Fortugno P, Bottillo I, Lopez M, Josselin E, Boudghene-Stambouli O, Agolini E, Bernardini L, Bellacchio E, Iannicelli M, Rossi A, Dib-Lachachi A, Stuppia L, Palka G, Mundlos S, Stricker S, Kornak U, Zambruno G, Dallapiccola B. Brancati F, et al. Among authors: stuppia l. Am J Hum Genet. 2010 Aug 13;87(2):265-73. doi: 10.1016/j.ajhg.2010.07.003. Am J Hum Genet. 2010. PMID: 20691405 Free PMC article.

2

Leukemic evolution in three patients with myelodysplastic syndrome and unusual chromosome changes.

Palka G, Calabrese G, Stuppia L, Guanciali Franchi P, Antonucci A, Spadano A, Di Lorenzo R, Torlontano G. Palka G, et al. Among authors: stuppia l. Cancer Genet Cytogenet. 1992 Jul 15;61(2):162-4. doi: 10.1016/0165-4608(92)90081-i. Cancer Genet Cytogenet. 1992. PMID: 1638498

3

Cytogenetic survey of 31 patients treated with bone marrow transplantation for acute nonlymphocytic and acute lymphoblastic leukemias.

Palka G, Calabrese G, Di Girolamo G, Stuppia L, Di Bartolomeo P, Guanciali Franchi P, Di Virgilio C, Bianchi GP, Angrilli F, Parruti G, et al. Palka G, et al. Among authors: stuppia l. Cancer Genet Cytogenet. 1991 Feb;51(2):223-33. doi: 10.1016/0165-4608(91)90135-h. Cancer Genet Cytogenet. 1991. PMID: 1993307

4

AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes.

Stuppia L, Romagno D, Palka G, Guanciali Franchi P, Parruti G, Calabrese G, Bianchi U. Stuppia L, et al. Cytogenet Cell Genet. 1991;56(1):59-60. doi: 10.1159/000133047. Cytogenet Cell Genet. 1991. PMID: 2004559

5

Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome?

Napolitano G, Palka G, Lio S, Bucci I, De Remigis P, Stuppia L, Monaco F. Napolitano G, et al. Among authors: stuppia l. Ann Genet. 1990;33(1):9-15. Ann Genet. 1990. PMID: 2142391

6

Cytogenetic study of the heterochromatic polymorphisms in 100 subjects with Down syndrome and their parents.

Palka G, Ciccotelli M, Sabatino G, Calabrese G, Guanciali Franchi P, Stuppia L, Parruti G, Di Virgilio C, Di Sante O. Palka G, et al. Among authors: stuppia l. Am J Med Genet Suppl. 1990;7:201-3. doi: 10.1002/ajmg.1320370741. Am J Med Genet Suppl. 1990. PMID: 2149948

7

Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation.

Calabrese G, Di Bartolomeo P, Stuppia L, Guanciali Franchi P, Parruti G, Ciancarelli M, Angrilli F, Geraci L, Palka G. Calabrese G, et al. Among authors: stuppia l. Cancer Genet Cytogenet. 1989 Aug;41(1):49-59. doi: 10.1016/0165-4608(89)90107-6. Cancer Genet Cytogenet. 1989. PMID: 2670196

8

A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22.

Parruti G, Di Ilio C, Calabrese G, Stuppia L, Guanciali Franchi P, Aceto A, Palka G. Parruti G, et al. Among authors: stuppia l. Ann Genet. 1989;32(1):55-8. Ann Genet. 1989. PMID: 2751250

9

Chromosome changes in 19 patients with Waldenström's macroglobulinemia.

Palka G, Spadano A, Geraci L, Fioritoni G, Dragani A, Calabrese G, Guanciali Franchi P, Stuppia L. Palka G, et al. Among authors: stuppia l. Cancer Genet Cytogenet. 1987 Dec;29(2):261-9. doi: 10.1016/0165-4608(87)90237-8. Cancer Genet Cytogenet. 1987. PMID: 3119188

10

On chromosomal DNA modifications by chemical and physical treatment of C-bands.

Stuppia L, Calabrese G, Guanciali Franchi P, Ferrucci L, Palka G. Stuppia L, et al. Basic Appl Histochem. 1987;31(4):487-92. Basic Appl Histochem. 1987. PMID: 3442554

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