1. An Evidence-Based Model of Multidisciplinary Care for Patients and Families Affected by Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. (28th February 2010) Authors: Schaeffer, Traci L.; Tryggestad, Jeanie B.; Mallappa, Ashwini; Hanna, Adam E.; Krishnan, Sowmya; Chernausek, Steven D.; Chalmers, Laura J.; Reiner, William G.; Kropp, Brad P.; Wisniewski, Amy B. Other Names: Lee Peter Allen Academic Editor. Journal: International journal of pediatric endocrinology Issue: Volume 2010(2010) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An Evidence-Based Model of Multidisciplinary Care for Patients and Families Affected by Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. (28th February 2010) Authors: Schaeffer, Traci L.; Tryggestad, Jeanie B.; Mallappa, Ashwini; Hanna, Adam E.; Krishnan, Sowmya; Chernausek, Steven D.; Chalmers, Laura J.; Reiner, William G.; Kropp, Brad P.; Wisniewski, Amy B. Other Names: Lee Peter Allen Academic Editor. Journal: International journal of pediatric endocrinology Issue: Volume 2010(2010) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Corrigendum to "Management Challenges in a Child with Chronic Hyponatremia: Use of V2 Receptor Antagonist". (2nd July 2017) Authors: Krishnan, Sowmya; Deshpande, Swapna; Mallappa, Ashwini; Gunda, Divya; Lane, Pascale; Vishwanath, Anu; McNall-Knapp, Rene Y. Journal: Case reports in pediatrics Issue: Volume 2017(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Management Challenges in a Child with Chronic Hyponatremia: Use of V2 Receptor Antagonist. (9th January 2017) Authors: Krishnan, Sowmya; Deshpande, Swapna; Mallappa, Ashwini; Divya, Gunda; Lane, Pascale; Vishwanath, Anu; McNall-Knapp, Rene Y. Other Names: Li Albert M. Academic Editor. Journal: Case reports in pediatrics Issue: Volume 2017(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel compound heterozygous variants in the NBAS gene in a child with osteogenesis imperfecta and recurrent acute liver failure. Issue 2 (4th February 2021) Authors: Krishnan, Sowmya; Rughani, Ankur; Tsai, Anne; Palle, Sirish Journal: BMJ case reports Issue: Volume 14:Issue 2(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. SARS‐CoV‐2 infection and paediatric endocrine disorders: Risks and management considerations. Issue 3 (3rd June 2021) Authors: Miller, Ryan; Ashraf, Ambika P.; Gourgari, Evgenia; Gupta, Anshu; Kamboj, Manmohan K.; Kohn, Brenda; Lahoti, Amit; Mak, Daniel; Mehta, Shilpa; Mitchell, Deborah; Patel, Neha; Raman, Vandana; Reynolds, Danielle G.; Yu, Christine; Krishnan, Sowmya Journal: Endocrinology, diabetes & metabolism Issue: Volume 4:Issue 3(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding protein. (22nd January 2020) Authors: Rughani, Ankur; Zhang, Dongsheng; Vairamani, Kanimozhi; Dauber, Andrew; Hwa, Vivian; Krishnan, Sowmya Journal: Clinical endocrinology Issue: Volume 92:Number 4(2020) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗