Rani H Singh PhD

Contact Information:

Phone: 404-778-8519

Email: rsingh@emory.edu

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SOM: Hum Gen: Medical Genetics

School Of Medicine

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Works 1-10 of 21

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Bone health in phenylketonuria: a systematic review and meta-analysis

by Serwet Demirdas; Katie E. Coakley; Peter H. Bisschop; Carla E. M. Hollak; Annet M. Bosch; Rani Singh



Recommendations for the nutrition management of phenylalanine hydroxylase deficiency

by Rani H Singh; Fran Rohr; Dianne Frazier; Amy Cunningham; Shideh Mofidi; Beth Ogata; Patricia L. Splett; Kathryn Moseley; Kathleen Huntington; Phyllis B. Acosta; Jerry Vockley; Sandra C. Van Calcar



Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.

by Yin-Hsiu Chien; Jose E. Abdenur; Federico Baronio; Allison Anne Bannick; Fernando Corrales; Maria Couce; Markus G. Donner; Can Ficicioglu; Cynthia Freehauf; Deborah Frithiof; Garrett Gotway; Koichi Hirabayashi; Floris Hofstede; George Hoganson; Wuh-Liang Hwu; Philip James; Sook Kim; Stanley H. Korman; Robin Lachmann; Harvey Levy; Martin Lindner; Lilia Lykopoulou; Ertan Mayatepek; Ania Muntau; Yoshiyuki Okano; Kimiyo Raymond; Estela Rubio-Gozalbo; Sabine Scholl-Bürgi; Andreas Schulze; Rani Singh; Sally Stabler; Mary Stuy; Janet Thomas; Conrad Wagner; William G. Wilson; Saskia Wortmann; Shigenori Yamamoto; Maryland Pao; Henk J. Blom



Insurance coverage of medical foods for treatment of inherited metabolic disorders

by Susan A. Berry; Mary Kay Kenney; Katharine B. Harris; Rani H Singh; Cynthia A. Cameron; Jennifer N. Kraszewski; Jill Levy-Fisch; Jill F. Shuger; Carol L. Greene; Michele A. Lloyd-Puryear; Coleen A. Boyle



Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations

by Jeffrey M. Chinsky; Rani Singh; Can Ficicioglu; Clara D. M. van Karnebeek; Markus Grompe; Grant Mitchell; Susan E. Waisbren; Muge Gucsavas-Calikoglu; Melissa P. Wasserstein; Katie Coakley; C. Ronald Scott



Natural history of children and adults with maple syrup urine disease in the NBS-MSUD Connect registry

by Aileen Kenneson; Yetsa Osara; Theresa Pringle; Lauren Youngborg; Rani Singh