Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Teresa Sadeghin"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101308- (2024)
Externí odkaz:
https://doaj.org/article/6c7cba3ecbe448788517962195b27895
P224: An exploration of the neurodevelopmental phenotype of two patients with 48,XXYY during infancy
Autor:
Lindsey Lang, Andrea Gropman, Debra Counts, Antonie Kline, Francie Mitchell, Elizabeth Buscema, Teresa Sadeghin, Carole Samango-Sprouse
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100252- (2023)
Externí odkaz:
https://doaj.org/article/91edbfaef11046a9826f46be426be53f
Autor:
Carole Samango-Sprouse, Alexa Taylor, Debra Counts, Teresa Sadeghin, Lindsey Lang, Andrea Gropman
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100316- (2023)
Externí odkaz:
https://doaj.org/article/7b8a5f9fdbcb4567b2c731edf013b408
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100352- (2023)
Externí odkaz:
https://doaj.org/article/50db1fc222b54b49ae6a524bed1ea8e8
Autor:
Mary P. Hamzik, Andrea L. Gropman, Michaela R. Brooks, Sherida Powell, Teresa Sadeghin, Carole A. Samango-Sprouse
Publikováno v:
Genes, Vol 14, Iss 7, p 1402 (2023)
47,XXY, also known as Klinefelter syndrome, is the most commonly occurring sex chromosomal aneuploidy (SCA). Hormonal replacement therapy (HRT) has been associated with improved neurodevelopmental capabilities in boys with 47,XXY, although studies in
Externí odkaz:
https://doaj.org/article/532ada02ceab427eaac0ddce8481a4d8
Autor:
Carole A. Samango-Sprouse, Mary P. Hamzik, Kenneth Rosenbaum, Kosar Khaksari, Francie Mitchell, Ritika Kommareddi, Michaela R. Brooks, Elizabeth Tipton, Teresa Sadeghin, Andrea L. Gropman
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Pallister–Killian syndrome is an uncommon genetic disorder that has broad developmental and multisystemic effects. While medical complications are widely reported throughout the literature, research on the neurodevelopmental profile has been limite
Externí odkaz:
https://doaj.org/article/3e322b6a9d13490797006e3b3572b8e1
Autor:
Sophia Q. Song, Andrea Gropman, Robert W. Benjamin, Francie Mitchell, Michaela R. Brooks, Mary P. Hamzik, Kira Sampson, Ritika Kommareddi, Teresa Sadeghin, Carole A. Samango-Sprouse
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Congenital adrenal hyperplasia is a group of autosomal recessive disorders in which enzymes in the cortisol biosynthesis pathways are disrupted by gene mutations. The most common form of congenital adrenal hyperplasia, caused by 21-hydroxylase defici
Externí odkaz:
https://doaj.org/article/052e3e09f55845b3aa15aa9dfa52ee8c
Autor:
Samango-Sprouse, Mary P. Hamzik, Andrea L. Gropman, Michaela R. Brooks, Sherida Powell, Teresa Sadeghin, Carole A.
Publikováno v:
Genes; Volume 14; Issue 7; Pages: 1402
47,XXY, also known as Klinefelter syndrome, is the most commonly occurring sex chromosomal aneuploidy (SCA). Hormonal replacement therapy (HRT) has been associated with improved neurodevelopmental capabilities in boys with 47,XXY, although studies in
Autor:
Carole A. Samango-Sprouse, Mary P. Hamzik, Eliana Gropman, Michaela R. Brooks, Sherida Powell, Alexa M. Taylor, Teresa Sadeghin, Andrea L. Gropman
Publikováno v:
Genetics in Medicine. 25:100847
Autor:
Michaela Reiko Brooks, Andrea Lynne Gropman, Mary Pat Hamzik, Kosar Khaksari, Sherida Powell, Teresa Sadeghin, Alexa Marie Taylor, Carole Samango-Sprouse
Publikováno v:
Genetics in Medicine. :100864