Regarding the consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. Creighton, S., Ransley, P., Duffy, P., Wilcox, D., Mushtaq, I., Cuckow, P., Woodhouse, C., Minto, C., Crouch, N., Stanhope, R., Hughes, I., Dattani, M., Hindmarsh, P., Brain, C., Achermann, J., Conway, G., Liao, L. M., Barnicoat, A., & Perry, L. The Journal of clinical endocrinology and metabolism, 88(7):3455; author reply 3456, July, 2003. bibtex
Downloads: 0
{"_id":"4dMQt9o5Ntdu39k89","bibbaseid":"creighton-ransley-duffy-wilcox-mushtaq-cuckow-woodhouse-minto-etal-regardingtheconsensusstatementon21hydroxylasedeficiencyfromthelawsonwilkinspediatricendocrinesocietyandtheeuropeansocietyforpaediatricendocrinology-2003","author_short":["Creighton, S.","Ransley, P.","Duffy, P.","Wilcox, D.","Mushtaq, I.","Cuckow, P.","Woodhouse, C.","Minto, C.","Crouch, N.","Stanhope, R.","Hughes, I.","Dattani, M.","Hindmarsh, P.","Brain, C.","Achermann, J.","Conway, G.","Liao, L. M.","Barnicoat, A.","Perry, L."],"bibdata":{"bibtype":"article","type":"article","title":"Regarding the consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology","volume":"88","issn":"0021-972X","language":"eng","number":"7","journal":"The Journal of clinical endocrinology and metabolism","author":[{"propositions":[],"lastnames":["Creighton"],"firstnames":["Sarah"],"suffixes":[]},{"propositions":[],"lastnames":["Ransley"],"firstnames":["Philip"],"suffixes":[]},{"propositions":[],"lastnames":["Duffy"],"firstnames":["Patrick"],"suffixes":[]},{"propositions":[],"lastnames":["Wilcox"],"firstnames":["Duncan"],"suffixes":[]},{"propositions":[],"lastnames":["Mushtaq"],"firstnames":["Imran"],"suffixes":[]},{"propositions":[],"lastnames":["Cuckow"],"firstnames":["Peter"],"suffixes":[]},{"propositions":[],"lastnames":["Woodhouse"],"firstnames":["Christopher"],"suffixes":[]},{"propositions":[],"lastnames":["Minto"],"firstnames":["Catherine"],"suffixes":[]},{"propositions":[],"lastnames":["Crouch"],"firstnames":["Naomi"],"suffixes":[]},{"propositions":[],"lastnames":["Stanhope"],"firstnames":["Richard"],"suffixes":[]},{"propositions":[],"lastnames":["Hughes"],"firstnames":["Ieuan"],"suffixes":[]},{"propositions":[],"lastnames":["Dattani"],"firstnames":["Mehul"],"suffixes":[]},{"propositions":[],"lastnames":["Hindmarsh"],"firstnames":["Peter"],"suffixes":[]},{"propositions":[],"lastnames":["Brain"],"firstnames":["Caroline"],"suffixes":[]},{"propositions":[],"lastnames":["Achermann"],"firstnames":["John"],"suffixes":[]},{"propositions":[],"lastnames":["Conway"],"firstnames":["Gerard"],"suffixes":[]},{"propositions":[],"lastnames":["Liao"],"firstnames":["Lih","Mei"],"suffixes":[]},{"propositions":[],"lastnames":["Barnicoat"],"firstnames":["Angela"],"suffixes":[]},{"propositions":[],"lastnames":["Perry"],"firstnames":["Les"],"suffixes":[]}],"month":"July","year":"2003","pmid":"12843205","keywords":"Adrenal Hyperplasia, Congenital, Child, Consensus, Endocrinology, Europe, Female, Gender Identity, Genitalia, Humans, Male, Pediatrics, Societies, Medical, Steroid 21-Hydroxylase","pages":"3455; author reply 3456","author_short":["Creighton, S.","Ransley, P.","Duffy, P.","Wilcox, D.","Mushtaq, I.","Cuckow, P.","Woodhouse, C.","Minto, C.","Crouch, N.","Stanhope, R.","Hughes, I.","Dattani, M.","Hindmarsh, P.","Brain, C.","Achermann, J.","Conway, G.","Liao, L. M.","Barnicoat, A.","Perry, L."],"key":"creighton_regarding_2003-1","id":"creighton_regarding_2003-1","bibbaseid":"creighton-ransley-duffy-wilcox-mushtaq-cuckow-woodhouse-minto-etal-regardingtheconsensusstatementon21hydroxylasedeficiencyfromthelawsonwilkinspediatricendocrinesocietyandtheeuropeansocietyforpaediatricendocrinology-2003","role":"author","urls":{},"keyword":["Adrenal Hyperplasia","Congenital","Child","Consensus","Endocrinology","Europe","Female","Gender Identity","Genitalia","Humans","Male","Pediatrics","Societies","Medical","Steroid 21-Hydroxylase"],"metadata":{"authorlinks":{}},"html":""},"bibtype":"article","biburl":"https://bibbase.org/zotero/MichalRaz","dataSources":["PJeWnMTsRzaEwoJmn"],"keywords":["adrenal hyperplasia","congenital","child","consensus","endocrinology","europe","female","gender identity","genitalia","humans","male","pediatrics","societies","medical","steroid 21-hydroxylase"],"search_terms":["regarding","consensus","statement","hydroxylase","deficiency","lawson","wilkins","pediatric","endocrine","society","european","society","paediatric","endocrinology","creighton","ransley","duffy","wilcox","mushtaq","cuckow","woodhouse","minto","crouch","stanhope","hughes","dattani","hindmarsh","brain","achermann","conway","liao","barnicoat","perry"],"title":"Regarding the consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology","year":2003}