Results 21 to 30 of about 167,087,863 (243)
FGF9 and WNT4 act as antagonistic signals to regulate mammalian sex determination [PDF]
, 2006 The genes encoding members of the wingless-related MMTV integration site (WNT) and fibroblast growth factor (FGF) families coordinate growth, morphogenesis, and differentiation in many fields of cells during development.Robin Lovell-Badge, Sekido, R, Behringer, Richard R, Capel, Blanche, Lovell-Badge, R, DiNapoli, Leo, Blanche Capel, Chaboissier, Marie-Christine, Behringer Richard R, Lovell-Badge, Robin, DiNapoli Leo, Poulat Francis, Behringer, RR, Kim Yuna, Kobayashi, Akio, Poulat, F, Behringer, Richard,, Behringer, Richard, R., Brennan, J, Chaboissier, M-C, Capel, B, Leo DiNapoli, Ryohei Sekido, Kim, Y, Kim, Yuna, Yuna Kim, Marie-Christine Chaboissier, Francis Poulat, Jennifer Brennan, Lovell-Badge Robin, Akio Kobayashi, Kobayashi Akio, DiNapoli, L, Brennan Jennifer, Capel Blanche, Kobayashi, A, Brennan, Jennifer, Richard R Behringer, Poulat, Francis, Chaboissier Marie-Christine, Sekido, Ryohei, Sekido Ryohei +41 morecore +1 more source408 Cases of Genital Ambiguity Followed by Single Multidisciplinary Team during 23 Years: Etiologic Diagnosis and Sex of Rearing
International Journal of Endocrinology, 2016 Objective. To evaluate diagnosis, age of referral, karyotype, and sex of rearing of cases with disorders of sex development (DSD) with ambiguous genitalia. Methods. Retrospective study during 23 years at outpatient clinic of a referral center.Georgette Beatriz De Paula, Beatriz Amstalden Barros, Stela Carpini, Bruna Jordan Tincani, Tais Nitsch Mazzola, Mara Sanches Guaragna, Cristiane Santos da Cruz Piveta, Laurione Candido de Oliveira, Juliana Gabriel Ribeiro Andrade, Guilherme Guaragna-Filho, Pedro Perez Barbieri, Nathalia Montibeler Ferreira, Marcio Lopes Miranda, Ezequiel Moreira Gonçalves, Andre Moreno Morcillo, Nilma Lucia Viguetti-Campos, Sofia Helena Valente Lemos-Marini, Roberto Benedito de Paiva Silva, Antonia Paula Marques-de-Faria, Maricilda Palandi De Mello, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior +21 moredoaj +1 more sourceIncreased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia [PDF]
, 2013 © 2013 Mac Keith Press.Sex chromosome aneuploidies increase the risk of spoken or written language disorders but individuals with specific language impairment (SLI) or dyslexia do not routinely undergo cytogenetic analysis. We assess the frequency of sex Newbury, Dianne F, Bolton, Patrick F, Knight, JC, Paracchini, S., Simpson, N., Simkin, Z., Talcott, J., Scerri, TS, O'Hare, A., Newbury, D., Addis, Laura, Knight, Julian, Fairfax, Benjamin P, Pickles, A, Clark, A., Bishop, D. V M, Seckl, J, Talcott, JB, Addis, L., Stein, J., Nasir, J, Knight, J., Nudel, R, Knight, Julian C, Stein, J, Monaco, AP, Slonims, V., Fairfax, Benjamin P., Slonims, Vicky, O'Hare, Anne, O'Hare, A, Simkin, Z, Addis, L, ?, ?, Pickles, A., Brandler, WM, Everitt, A., Hennessy, ER, Stein, John, Everitt, A, Watson, J, Clark, Ann, Fairfax, BP, Cohen, W., Cowie, H., Conti-Ramsden, G., Cohen, W, Paracchini, Silvia, Watson, J., Simpson, Nuala H, Stein, John F., Hennessy, Elizabeth R., Nudel, R., Seckl, J., Bolton, PF, Scerri, Thomas S, Baird, Gillian, Hennessy, E., Simpson, Nuala H., Talcott, Joel B., Talcott, Joel B, Baird, G., SLI Consortium, Brandler, W., Fisher, Simon E, Consortium, Sli, Brandler, William M., Baird, G, Fairfax, B., Knight, Julian C., Fisher, S., Nasir, J., Fisher, SE, Simpson, NH, Conti-Ramsden, G, Conti-Ramsden, Gina, Monaco, A. P., Cowie, H, Hennessy, Elizabeth R, Paracchini, S, Scerri, T., Slonims, V, Clark, A, Bishop, DVM, Watson, Jocelynne, Newbury, Dianne F., Simonoff, E, Brandler, William M, Simonoff, E., Newbury, DF, Fisher, Simon E., Scerri, Thomas S., Bolton, Patrick F. +92 morecore +1 more sourceUK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development [PDF]
, 2011 It is paramount that any child or adolescent with a suspected disorder of sex development (DSD) is assessed by an experienced clinician with adequate knowledge about the range of conditions associated with DSD.Wallace, A. Michael, Miles, HL, Louise Izatt, Michael Wallace, A, A. Michael Wallace, Sue Elford, Sanders, C, Simmonds, M, Edwards, Zoe, Gerry Conway, Elford, S, Watt, Andrew, Les Perry, John C. Achermann, Sanders, C., O'Toole, S, Balen, Adam, Balen, A.H., Miles, H.L., Miles, Harriet L., Sanders, Caroline, Krone, Nils, Izatt, L, Willis, Debbie, Ieuan A. Hughes, Arl, W, Adam H. Balen, Arlt, W., Wiebke Arlt, Willis, D, Debbie Willis, Ahmed, S.F., S. Faisal Ahmed, Edwards, ZL, Edwards, Z.L., Hughes, Ieuan A., Perry, Les, Margaret Simmonds, O'Toole, S., Ahmed, SF, Faisal Ahmed, S, Achermann, John C, Elford, Sue, Conway, Gerry, Wallace, AM, Edwards, Zoe L., Miles, Harriet, Willis, D., Wallace, A.M., Watt, A., Nils Krone, Hughes, I.A., Simmonds, M., Achermann, JC, Izatt, Louise, O'Toole, Stuart, Hughes, IA, Krone, N, Perry, L., Simmonds, Margaret, Balen, AH, Hughes, Ieuan A, Elford, S., Conway, G., Ahmed, S. Faisal, Zoe L. Edwards, Stuart O’Toole, Krone, N., Perry, L, Arlt, Wiebke, Caroline Sanders, Andrew Watt, Achermann, John C., Balen, Adam H., O’Toole, Stuart, Achermann, J.C., Harriet L. Miles, Conway, G, Izatt, L., Watt, A +79 morecore +1 more sourceTowards a virtual research environment for paediatric endocrinology across Europe [PDF]
, 2009 Paediatric endocrinology is a medical specialty dealing with variations of physical growth and sexual development in childhood. Genetic anomalies that can cause disorders of sexual development in children are rare.Jiang, J., John Watt, Watt, J., Anthony Stell, Watt, J, Ahmed, F., Jiang, J, Sinnott, R, Jipu Jiang, Richard Sinnott, Sinnott, R.O., Stell, A, Stell, A., Faisal Ahmed, Ahmed, F +14 morecore +1 more sourceDisorders/Differences of Sex Development Presenting in the Newborn With 46,XY Karyotype
Frontiers in Pediatrics, 2021 Differences/disorders of sex development (DSD) are a heterogeneous group of congenital conditions, resulting in discordance between an individual's sex chromosomes, gonads, and/or anatomic sex. The management of a newborn with suspected 46,XY DSD remains Silvano Bertelloni, Nina Tyutyusheva, Margherita Valiani, Franco D'Alberton, Fulvia Baldinotti, Maria Adelaide Caligo, Giampiero I. Baroncelli, Diego G. Peroni +7 moredoaj +1 more sourceAdditional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development
Reproductive Biology and Endocrinology, 2023 Background Forty-six ,XY Differences/Disorders of Sex Development (DSD) are characterized by a broad phenotypic spectrum ranging from typical female to male with undervirilized external genitalia, or more rarely testicular regression with a typical male ...Khouloud Rjiba, Soumaya Mougou-Zerelli, Imen hadj Hamida, Ghada Saad, Bochra Khadija, Afef Jelloul, Wafa Slimani, Yosra Hasni, Sarra Dimassi, Hela Ben khelifa, Amira Sallem, Molka Kammoun, Hamza Hadj Abdallah, Moez Gribaa, Joelle Bignon-Topalovic, Sami Chelly, Hédi Khairi, Mohamed Bibi, Maha Kacem, Ali Saad, Anu Bashamboo, Kenneth McElreavey +21 moredoaj +1 more source