Silvana Caiulo
Overview
Explore the profile of Silvana Caiulo including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
277
Followers
0
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Recent Articles
1.
Ferrigno R, Hasenmajer V, Caiulo S, Minnetti M, Mazzotta P, Storr H, et al.
Rev Endocr Metab Disord
. 2021 Jan;
22(4):817-835.
PMID: 33515368
Cushing's disease (CD) is rare in paediatric practice but requires prompt investigation, diagnosis and therapy to prevent long-term complications. Key presenting features are a change in facial appearance, weight gain,...
2.
Kostopoulou E, Dastamani A, Guemes M, Clement E, Caiulo S, Shanmugananda P, et al.
Clin Endocrinol (Oxf)
. 2020 Dec;
94(3):399-412.
PMID: 33345357
Objective: Hyperinsulinaemic hypoglycaemia (HH) is one of the commonest causes of hypoglycaemia in children. The molecular basis includes defects in pathways that regulate insulin release. Syndromic conditions like Beckwith-Wiedemann (BWS),...
3.
Caiulo S, Corbetta C, DI Frenna M, Medda E, De Angelis S, Rotondi D, et al.
J Clin Endocrinol Metab
. 2020 Oct;
106(1):e338-e349.
PMID: 33124651
Context: Analysis of a 2-screen program for congenital hypothyroidism (CH) was performed using differential dried-blood spot thyrotropin (bTSH) cutoffs of 10 mU/L at first screening (all infants) and 5 mU/L...
4.
Minnetti M, Caiulo S, Ferrigno R, Baldini-Ferroli B, Bottaro G, Gianfrilli D, et al.
Clin Endocrinol (Oxf)
. 2019 Nov;
92(2):98-108.
PMID: 31747461
Abnormal adrenal function can interfere with linear growth, potentially causing either acceleration or impairment of growth in paediatric patients. These abnormalities can be caused by direct effects of adrenal hormones,...
5.
Medda E, Vigone M, Cassio A, Calaciura F, Costa P, Weber G, et al.
J Clin Endocrinol Metab
. 2019 Jul;
104(12):5765-5779.
PMID: 31287502
Context: Newborn screening program for congenital hypothyroidism (CH) adopting rescreening in at-risk neonates. Objectives: To estimate the concordance rate for CH in twin pairs discordant at the first screening; to...
6.
Kostopoulou E, Dastamani A, Caiulo S, Antell H, Flanagan S, Shah P
Clin Endocrinol (Oxf)
. 2019 Feb;
90(5):766-769.
PMID: 30776145
No abstract available.
7.
Nimri R, Dassau E, Segall T, Muller I, Bratina N, Kordonouri O, et al.
Diabetes Obes Metab
. 2018 Jun;
20(10):2458-2466.
PMID: 29885025
Aims: To evaluate physicians' adjustments of insulin pump settings based on continuous glucose monitoring (CGM) for patients with type 1 diabetes and to compare these to automated insulin dose adjustments....
8.
Vigone M, DI Frenna M, Guizzardi F, Gelmini G, de Filippis T, Mora S, et al.
Clin Endocrinol (Oxf)
. 2017 Jun;
87(5):587-596.
PMID: 28561265
Objective: Mutations in TSH receptor (TSHR) are associated with TSH resistance, a genetic defect characterized by a heterogeneous phenotype ranging from severe hypothyroidism to subclinical hypothyroidism (SCH). We assessed the...
9.
Caiulo V, Gargani L, Caiulo S, Fisicaro A, Moramarco F, Latini G, et al.
Pediatr Pulmonol
. 2014 Feb;
49(6):619-20.
PMID: 24532447
No abstract available.
10.
Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidism
Vigone M, Caiulo S, DI Frenna M, Ghirardello S, Corbetta C, Mosca F, et al.
J Pediatr
. 2014 Feb;
164(6):1296-302.
PMID: 24518164
Objective: To determine the evolution of congenital hypothyroidism in preterms and the clinical features of permanent forms. Study Design: We retrospectively evaluated 24 preterm children detected by newborn screening for...