1. A novel de novo frameshift mutation in NR0B1 and low prenatal estriol in adrenal hypoplasia congenita. Issue 1 (21st August 2018) Authors: Khattab, Ahmed; Nelson‐Williams, Carol; Cabreza, Vivienne; Macdonald, Anne; Loring, Erin; Saland, Jeffrey; New, Maria I. Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1433:Issue 1(2018) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred. Issue 1 (15th August 2016) Authors: Yau, Mabel; Azkawi, Hanan Said Al; Haider, Shozeb; Khattab, Ahmed; Badi, Maryam Al; Abdullah, Wafa; Senani, Aisha Al; Wilson, Robert C.; Yuen, Tony; Zaidi, Mone; New, Maria I. Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1376:Issue 1(2016) Page Start: 65 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype–phenotype nonconcordance. Issue 1 (20th August 2015) Authors: Khattab, Ahmed; Yuen, Tony; Al‐Malki, Sultan; Yau, Mabel; Kazmi, Diya; Sun, Li; Harbison, Madeleine; Haider, Shozeb; Zaidi, Mone; New, Maria I. Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1364:Issue 1(2016) Page Start: 5 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Apparent mineralocorticoid excess and the long term treatment of genetic hypertension. Issue 165 (January 2017) Authors: Razzaghy-Azar, Maryam; Yau, Mabel; Khattab, Ahmed; New, Maria I. Journal: Journal of steroid biochemistry and molecular biology Issue: Issue 165:Part A(2017) Page Start: 145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Beyond bone biology: Lessons from team science. Issue 11 (22nd July 2020) Authors: Zaidi, Mone; Lizneva, Daria; Gera, Sakshi; Taneja, Charit; Korkmaz, Funda; Gumerova, Anisa; Ievleva, Kseniia; Ahmad, Naseer; Ryu, Vitaly; Sun, Li; Kim, Se‐Min; New, Maria I.; Haider, Shozeb; Iqbal, Jameel; Rosen, Clifford; Yuen, Tony Journal: Journal of orthopaedic research Issue: Volume 38:Issue 11(2020) Page Start: 2331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Blocking FSH Induces Thermogenic Adipose Tissue and Reduces Body Fat. Issue 10 (October 2017) Authors: Liu, Peng; Ji, Yaoting; Yuen, Tony; Rendina-Ruedy, Elizabeth; DeMambro, Victoria E.; Dhawan, Samarth; Abu-Amer, Wahid; Izadmehr, Sudeh; Zhou, Bin; Shin, Andrew C.; Latif, Rauf; Thangeswaran, Priyanthan; Gupta, Animesh; Li, Jianhua; Shnayder, Valeria; Robinson, Samuel T.; Yu, Yue Eric; Zhang, Xing... Journal: Obstetrical & gynecological survey Issue: Volume 72:Issue 10(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype. Issue 1 (22nd June 2017) Authors: Gurgov, Semyon; Bernabé, Kerlly J.; Stites, John; Cunniff, Christopher M.; Lin‐Su, Karen; Felsen, Diane; New, Maria I.; Poppas, Dix P. Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1402:Issue 1(2017) Page Start: 56 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Long term outcomes in 46, XX adult patients with congenital adrenal hyperplasia reared as males. Issue 165 (January 2017) Authors: Khattab, A.; Yau, M.; Qamar, A.; Gangishetti, P.; Barhen, A.; Al-Malki, S.; Mistry, H.; Anthony, W.; Toralles, M.B; New, Maria I. Journal: Journal of steroid biochemistry and molecular biology Issue: Issue 165:Part A(2017) Page Start: 12 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia. Issue 165 (January 2017) Authors: Dumic, Katja K.; Grubic, Zorana; Yuen, Tony; Wilson, Robert C.; Kusec, Vesna; Barisic, Ingeborg; Stingl, Katarina; Sansovic, Ivona; Skrabic, Veselin; Dumic, Miroslav; New, Maria I. Journal: Journal of steroid biochemistry and molecular biology Issue: Issue 165:Part A(2017) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Issue 165 (January 2017) Authors: Parsa, Alan A.; New, Maria I. Journal: Journal of steroid biochemistry and molecular biology Issue: Issue 165:Part A(2017) Page Start: 2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗