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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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D Capalbo

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Journal of Endocrinological Investigation|June 6, 2009

A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiencyY Carlomagno, M Salerno, D Vivenza, et al.

Journal of Pediatric Urology|December 12, 2018

'Frequently recurring' nocturnal polyuria is predictive of response to desmopressin in monosymptomatic nocturnal enuresis in childhoodP Marzuillo, R Marotta, S Guarino, et al.

Journal of Endocrinological Investigation|November 10, 2010

Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.

Journal of Endocrinological Investigation|May 18, 2021

Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patientsS Garelli, M Dalla Costa, C Sabbadin, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Journal of Endocrinological Investigation|June 6, 2009

A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiencyY Carlomagno, M Salerno, D Vivenza, et al.

Journal of Pediatric Urology|December 12, 2018

'Frequently recurring' nocturnal polyuria is predictive of response to desmopressin in monosymptomatic nocturnal enuresis in childhoodP Marzuillo, R Marotta, S Guarino, et al.

Journal of Endocrinological Investigation|November 10, 2010

Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.

Journal of Endocrinological Investigation|May 18, 2021

Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patientsS Garelli, M Dalla Costa, C Sabbadin, et al.

Pageof 2