Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Melina Dendrinos"'
Autor:
Jessica Duis, Mark Nespeca, Jane Summers, Lynne Bird, Karen G.C.B. Bindels‐de Heus, M. J. Valstar, Marie‐Claire Y. deWit, C. Navis, Maartje ten Hooven‐Radstaake, Bianca M. vanIperen‐Kolk, Susan Ernst, Melina Dendrinos, Terry Katz, Gloria Diaz‐Medina, Akshat Katyayan, Srishti Nangia, Ronald Thibert, Daniel Glaze, Christopher Keary, Karine Pelc, Nicole Simon, Anjali Sadhwani, Helen Heussler, Anne Wheeler, Caroline Woeber, Margaret DeRamus, Amy Thomas, Emily Kertcher, Lauren DeValk, Kristen Kalemeris, Kara Arps, Carol Baym, Nicole Harris, John P. Gorham, Brenda L. Bohnsack, Reid C. Chambers, Sarah Harris, Henry G. Chambers, Katherine Okoniewski, Elizabeth R. Jalazo, Allyson Berent, Carlos A. Bacino, Charles Williams, Anne Anderson
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Background Angelman syndrome (AS) is a rare neurogenetic disorder present in approximately 1/12,000 individuals and characterized by developmental delay, cognitive impairment, motor dysfunction, seizures, gastrointestinal concerns, and abnor
Externí odkaz:
https://doaj.org/article/eb69721114bc440fbbb670148e293148
Autor:
Melina Dendrinos, Olivia K. Winfrey, Anastasia L. Hryhorczuk, Elisabeth H. Quint, Y. Frances Fei
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 35:383-386
Background : The definitive treatment of distal vaginal atresia is surgery, but menstrual suppression is often helpful for initial management. Case : A 13-year-old presented with primary amenorrhea and progressive abdominal pain. She was diagnosed wi
Autor:
Jessica Duis, Mark Nespeca, Jane Summers, Lynne Bird, Karen G.C.B. Bindels‐de Heus, M. J. Valstar, Marie‐Claire Y. Wit, C. Navis, Maartje ten Hooven‐Radstaake, Bianca M. Iperen‐Kolk, Susan Ernst, Melina Dendrinos, Terry Katz, Gloria Diaz‐Medina, Akshat Katyayan, Srishti Nangia, Ronald Thibert, Daniel Glaze, Christopher Keary, Karine Pelc, Nicole Simon, Anjali Sadhwani, Helen Heussler, Anne Wheeler, Caroline Woeber, Margaret DeRamus, Amy Thomas, Emily Kertcher, Lauren DeValk, Kristen Kalemeris, Kara Arps, Carol Baym, Nicole Harris, John P. Gorham, Brenda L. Bohnsack, Reid C. Chambers, Sarah Harris, Henry G. Chambers, Katherine Okoniewski, Elizabeth R. Jalazo, Allyson Berent, Carlos A. Bacino, Charles Williams, Anne Anderson
Publikováno v:
Molecular geneticsgenomic medicine. 10(3)
Background: Angelman syndrome (AS) is a rare neurogenetic disorder present in approximately 1/12,000 individuals and characterized by developmental delay, cognitive impairment, motor dysfunction, seizures, gastrointestinal concerns, and abnormal elec
Publikováno v:
Journal of pediatric and adolescent gynecology. 35(5)
Traumatic non-obstetrical hematomas of the vulva are rare, and most reports only involve adult patients. There are no data on presentation, management, and outcomes from either conservative or surgical management in pediatric and adolescent patients.
Autor:
Olivia Winfrey, Mina Farahzad, Elisabeth Quint, Yolanda Smith, Monica Rosen, Melina Dendrinos
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 35:220-221
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 35:233-234
Publikováno v:
Journal of pediatric and adolescent gynecology. 34(4)
To characterize the patient population with cognitive or physical impairments that presents for anticipatory guidance of puberty, evaluate caregiver concerns with respect to puberty, and describe chosen management strategies and outcomes following me
Publikováno v:
The Journal of adolescent health : official publication of the Society for Adolescent Medicine. 69(3)
To characterize the population of adolescents and young women with special needs presenting for gynecologic care, describe usage patterns of hormonal suppression methods, and evaluate outcomes of menstrual management.This retrospective cohort study i
Autor:
Monica W. Rosen, Yueyang Fei, Julian Wan, Elisabeth H. Quint, Yolanda R. Smith, Olivia K. Winfrey, Melina Dendrinos
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 34:245-246
Background Despite the well-established embryological relationship in the development of renal and Mullerian structures, no guidelines exist regarding screening for Mullerian anomalies (MA) in the setting of a renal anomaly (RA). Delayed diagnosis of
Autor:
Chelsea Chase, Yolanda R. Smith, Melina Dendrinos, Yueyang Fei, Elisabeth H. Quint, Monica W. Rosen, Kelsey Carman
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 34:251-252
Background There are many reasons for choosing the etonogestrel subdermal implant (hereafter “implant”). Limited data exists on outcomes of implant use in adolescents, and specifically, on the management of abnormal uterine bleeding (AUB). The go