Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Jill D Jacobson"'
Publikováno v:
World Allergy Organization Journal, Vol 6, Iss , Pp - (2013)
Background McCune Albright syndrome (MAS) is a rare disorder characterized by precocious puberty, café-au-lait spots, and fibrous dysplasia. Its cause is an activating mutation in the GNAS gene, encoding a subunit of the stimulatory G protein, Gsalp
Externí odkaz:
https://doaj.org/article/a3a5fc25d1a44a66864c11b50648a7d1
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Autoimmune polyglandular syndrome type 1 (APS1) is a progressive life-threatening illness with no known cure. Current treatments involve replacement of the hormone deficiencies that result from autoimmune destruction of multiple endocrine organs. We
Externí odkaz:
https://doaj.org/article/0aed60f4ca7444ec91a574968c31ee8c
Publikováno v:
LGBT health. 8(4)
Purpose: Early use of oxandrolone and gonadotropin-releasing hormone analogs has been shown to increase adult height in patients at risk for short stature, but use in trans-masculine (TM) youth to ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f144109aff6a829491ac7b152ad5d4a8
https://pubmed.ncbi.nlm.nih.gov/33819432
https://pubmed.ncbi.nlm.nih.gov/33819432
Publikováno v:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 16(1)
Individuals with 45,X mosaicism with Y chromosome material raised as boys are not diagnosed with Turner syndrome, a label restricted to phenotypic females. We sought to determine if boys with 45,X mosaicism had features consistent with Turner syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f630f4af1ba3bf6b50b463f69fcb8a
https://pubmed.ncbi.nlm.nih.gov/34515231
https://pubmed.ncbi.nlm.nih.gov/34515231
Autor:
Anna M. Egan, Michele Knoll, Joel F Koenig, Julie Strickland, John M. Gatti, Jill D. Jacobson
Publikováno v:
Journal of the Endocrine Society
Introduction: Differences of Sex Development (DSDs) encompass variations in formation of internal or external sex characteristics. Historically, sex assignment in children with DSDs depended on phenotype, and gender was thought to be malleable. Atten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a1724d80399e345ebad746bdda0647
https://doi.org/10.1210/jendso/bvaa046.627
https://doi.org/10.1210/jendso/bvaa046.627
Autor:
John Gatti, Carol J Saunders, Anna Egan, Jill D. Jacobson, Julie Strickland, Emily G. Farrow, Laurel K. Willig, Leslie L. Heckert
Publikováno v:
Endocrinology. 161
Differences of sex development (DSDs) are a constellation of conditions that result in genital ambiguity or complete sex reversal. Although determining the underlying genetic variants can affect clinical management, fewer than half of undermasculiniz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c30367ac17aabaa340dc07390114b89d
https://doi.org/10.1210/endocr/bqz015
https://doi.org/10.1210/endocr/bqz015
Publikováno v:
The Journal of adolescent health : official publication of the Society for Adolescent Medicine. 61(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d4e369d2c14c44208c23e850ce935a
https://pubmed.ncbi.nlm.nih.gov/29061235
https://pubmed.ncbi.nlm.nih.gov/29061235
Autor:
Frances Grimstad, Jill D. Jacobson
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 32:215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffd4f870cebff4686468a7eb0a669c6b
https://doi.org/10.1016/j.jpag.2019.02.053
https://doi.org/10.1016/j.jpag.2019.02.053
Autor:
Gathi, Abraham, Sun-Young, Ahn, Rasheda, Amin, Anne L., Angiolillo, Rami A., Ballout, Khadija, Belhassan, Michael J., Bennett, Julie, Berg, Ajay, Bhatia, Janetta, Bryksin, Carlos, Castillo-Pinto, Amaziah, Coleman, Ferdinand, Coste, Jeffrey G., Dawson, Edgard E., Delvin, Yaser, Diab, Dennis J., Dietzen, Marc T., DiSabella, Andrew C., Edmondson, Michael, Edzards, Thomas, Ferkol, Gabriela (Paula), Finkielstain, Mary E., Fournier, Andrea, Gaedigk, Uttam, Garg, Sarah K., Garwood, Emily L., Gill, Jorge L., Granadillo, Michael F., Guerrera, Shannon, Haymond, Paul S., Hiers, Alyssa, James, Janis M., Stoll, Jill D., Jacobson, Andrew, Janowski, Smita, Jha, Patricia M., Jones, Jami L., Josefson, Randall K., Julian, Lawrence, Jung, Sakil, Kulkarni, Finza, Latif, Courtney, Lawrence, Van, Leung-Pineda, Fabien, Magne, Stephen R., Master, Emily Riehm, Meier, Deborah, Merke, Asha, Moudgil, Khushbu, Patel, Wendy M., Paul, Rowena, Punzalan, Scott, Raskin, Kimiyo, Raymond, Alan T., Remaley, Mary, Revenis, Adelaide, Robb, Stephen M., Roper, Blachy J. Dávila, Saldaña, Maryam, Salehi, Tracy L., Sandritter, Hemant, Sharma, Troy, Tenney, Silvia, Tortorelli, Akshaya, Vachharajani, Guy, Van Vliet, Amy L., White, William E., Winter, Edward C.C., Wong
Publikováno v:
In Biochemical and Molecular Basis of Pediatric Disease Edition: Fifth Edition. 2021:xxxiii-xxxviii