L Guazzarotti
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Explore the profile of L Guazzarotti including associated specialties, affiliations and a list of published articles.
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11
Citations
87
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Recent Articles
1.
Iughetti L, Antoniazzi F, Giavoli C, Bona G, Aversa T, Greggio N, et al.
J Endocrinol Invest
. 2020 Jun;
44(3):493-503.
PMID: 32557273
Purpose: To investigate the long-term safety (primary endpoint) and effectiveness (secondary endpoint) of the somatropin biosimilar Omnitrope. Methods: PATRO Children is an ongoing, multicenter, observational, post-marketing surveillance study. Children who...
2.
Guazzarotti L, Tadini G, Mancini G, Sani I, Pisanelli S, Galderisi F, et al.
Clin Genet
. 2017 Oct;
93(3):693-698.
PMID: 28976000
Ectodermal dysplasias are a group of genetic disorders defined by ectodermal derivative impairment (EDI). To test the impact of the Wnt/beta-catenin pathway in the genetic screening of EDI, we performed...
3.
Guazzarotti L, Tadini G, Mancini G, Giglio S, Willoughby C, Callea M, et al.
Clin Genet
. 2014 Apr;
87(4):338-42.
PMID: 24724966
Ectodermal dysplasias (EDs) are a group of genetic disorders characterized by the abnormal development of the ectodermal-derived structures. X-linked hypohidrotic ectodermal dysplasia, resulting from mutations in ED1 gene, is the...
4.
Schindler A, Guazzarotti L, Mameli C, Urbani E, Mozzanica F, Guerrini L, et al.
Int J Pediatr Otorhinolaryngol
. 2013 Aug;
77(9):1606-8.
PMID: 23906991
The congenital vomer defect (CVD) is a rare and still partially unknown condition. Only few cases have been reported in the international literature and the large majority of them appeared...
5.
Zuccotti G, Mameli C, Trabattoni D, Beretta S, Biasin M, Guazzarotti L, et al.
J Biol Regul Homeost Agents
. 2013 Mar;
27(1):253-8.
PMID: 23489705
Acute respiratory tract infections (ARTIs) are the most frequent illnesses in pediatric age, frequently experienced in children with Down Syndrome (DS) due to the associated immune defects of both specific...
6.
Massa O, Meschi F, Caumo A, Cerutti F, Toni S, Cherubini V, et al.
Diabetologia
. 2001 Aug;
44(7):898-905.
PMID: 11508276
Aims/hypothesis: The aim of this study was to assess the prevalence of glucokinase gene mutations in Italian children with MODY and to investigate genotype/phenotype correlations of the mutants. Methods: Screening...
7.
Guazzarotti L, Fumelli P, Testa I, Pecora R, Panicari F, Bellanne-Chantelot C, et al.
J Pediatr Endocrinol Metab
. 2001 Jun;
14 Suppl 1:611-7.
PMID: 11393552
Maturity Onset Diabetes of the Young (MODY) is an autosomal dominant monogenic form of type 2 diabetes mellitus (DM) representing 5% of youth-onset DM in the Caucasian population. In young...
8.
Guazzarotti L, Bartolotta E, Chiarelli F
J Pediatr Endocrinol Metab
. 1999 Jul;
12(4):487-97.
PMID: 10417964
The differential diagnosis of hyperglycemia in childhood and adolescence has to take into consideration early-onset non-insulin-dependent diabetes, defined as maturity onset diabetes of the young (MODY). To date, mutations in...
9.
Guazzarotti L, Thivolet C, Tardivel I, Chevalier A, Carel J
J Autoimmun
. 1995 Dec;
8(6):901-14.
PMID: 8824714
To study the heterogeneity of islet cell antibodies (ICA), recombinant rat and human GAD65 expressed as bacterial fusion proteins were used to inhibit ICA reactivity in sera from recent onset...
10.
Carel J, Lahlou N, Guazzarotti L, Joubert-Collin M, Roger M, Colle M, et al.
Eur J Endocrinol
. 1995 Jun;
132(6):699-704.
PMID: 7788009
We evaluated the pituitary and gonadal suppression in 40 girls and nine boys treated with depot leuprorelin (3.75 mg sc if body weight > or = 20 kg, 1.87 mg...