Einaudi, S.
68  Ergebnisse:
Personensuche X
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1

POR polymorphisms are associated with 21 hydroxylase defici..:

Pecori Giraldi, F. ; Einaudi, S. ; Sesta, A....
Journal of Endocrinological Investigation.  44 (2021)  10 - p. 2219-2226 , 2021
 
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3

Phalangeal quantitative ultrasound in 1,719 children and ad..:

Mussa, A. ; Porta, F. ; Baldassarre, G....
Osteoporosis International.  23 (2011)  7 - p. 1987-1998 , 2011
 
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4

Thyroid diseases in patients treated during pre-puberty for..:

Corrias, Andrea ; Einaudi, S. ; Ricardi, U....
Journal of Endocrinological Investigation.  24 (2001)  6 - p. 387-392 , 2001
 
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5

Accuracy of Fine Needle Aspiration Biopsy of Thyroid Nodule..:

Corrias, A. ; Einaudi, S. ; Chiorboli, E....
The Journal of Clinical Endocrinology & Metabolism.  86 (2001)  10 - p. 4644-4648 , 2001
 
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7

Thyroid dysfunction as a late effect in childhood medullobl..:

Ricardi, U ; Corrias, A ; Einaudi, S...
International Journal of Radiation Oncology*Biology*Physics.  48 (2000)  3 - p. 182 , 2000
 
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9

Growth in Children With Noonan Syndrome and Effects of Grow..:

Libraro A ; D'Ascanio V ; Cappa M...
info:eu-repo/semantics/altIdentifier/pmid/35002956.  , 2021
 
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10

POR polymorphisms are associated with 21 hydroxylase defici..:

Pecori Giraldi, F ; Einaudi, S ; Sesta, A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421294/.  , 2021
 
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11

International practice of corticosteroid replacement therap..:

Bacila, I ; Freeman, N ; Daniel, E...
https://eprints.whiterose.ac.uk/170579/7/%5B1479683X%20-%20European%20Journal%20of%20Endocrinology%5D%20International%20practice%20of%20corticosteroid%20replacement%20therapy%20in%20congenital%20adrenal%20hyperplasia_%20data%20from%20the%20I-CAH%20registry.pdf.  , 2021
 
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12

POR polymorphisms are associated with 21 hydroxylase defici..:

Pecori Giraldi F ; Einaudi S ; Sesta A...
info:eu-repo/semantics/altIdentifier/pmid/33666875.  , 2021
 
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13

Teriparatide (rhPTH 1–34) treatment in the pediatric age: l..:

Tuli G ; Buganza R ; Tessaris D...
info:eu-repo/semantics/altIdentifier/pmid/31705387.  , 2019
 
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15

Heterozygous missense mutations in steroidogenic factor 1 (..:

Lin, L ; Philibert, P ; Ferraz-de-Souza, B...
https://discovery.ucl.ac.uk/id/eprint/147931/1/991.full.pdf.  , 2007
 
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