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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
Detection of apoptosis in peripheral blood cells of 31 subjects affected by Down syndrome before and after zinc therapy.
Antonucci A, Di Baldassarre A, Di Giacomo F, Stuppia L, Palka G. Antonucci A, et al. Among authors: stuppia l. Ultrastruct Pathol. 1997 Sep-Oct;21(5):449-52. doi: 10.3109/01913129709021944. Ultrastruct Pathol. 1997. PMID: 9273975
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
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
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis.
Calabrese G, Stuppia L, Mingarelli R, Guanciali Franchi P, Peila R, Morizio E, Antonucci A, Palka G. Calabrese G, et al. Among authors: stuppia l. Ann Genet. 1994;37(3):135-8. Ann Genet. 1994. PMID: 7847794
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature.
Palka G, Geraci L, Calabrese G, Stuppia L, Guanciali Franchi P, Parruti G, D'Antonio D, Fioritoni G. Palka G, et al. Among authors: stuppia l. Ann Genet. 1988;31(3):190-2. Ann Genet. 1988. PMID: 3066283 Review.
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy.
Stuppia L, Gatta V, Gaspari AR, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Eur J Hum Genet. 2002 Jun;10(6):388-90. doi: 10.1038/sj.ejhg.5200819. Eur J Hum Genet. 2002. PMID: 12080391
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly.
Celentano C, Guanciali-Franchi PE, Liberati M, Palka C, Fantasia D, Morizio E, Calabrese G, Stuppia L, Rotmensch S. Celentano C, et al. Among authors: stuppia l. Prenat Diagn. 2005 Mar;25(3):220-4. doi: 10.1002/pd.1110. Prenat Diagn. 2005. PMID: 15791663
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
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.
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