1984
- Doty RL, Shaman P, Dann M. Development of the University of Pennsylvania Smell Identification Test: a standardized microencapsulated test of olfactory function. Physiol Behav. 1984 Mar;32(3):489-502. (UPSIT)
1993
- Yousem DM, Turner WJ, Li C, Snyder PJ, Doty RL. Kallmann syndrome: MR evaluation of olfactory system. Amer J Neuroradiol. 1993 Jul-Aug; 14(4): 839-43.
2007
- Versiani BR, Trarbach E, Koenigkam-Santos M, Dos Santos AC, Elias LL, Moreira AC, Latronico AC, de Castro M. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism. Clin Endocrinol (Oxf). 2007 Feb;66(2): 173-9. (SIT)
- Ahmad AT, Jbara MA, Hiyasat D, Bateiha A, Ajlouni KM. The standard clinical smell testing protocol of the National Center for Diabetes, Endocrinology and Genetics in Amman, Jordan: JOR test. Am J Otolaryngol. 2007 Nov-Dec; 28(6): 388-91. (UPSIT)
- Hasan KS, Reddy SS, Barsony N. Taste perception in kallmann syndrome, a model of congenital anosmia. Endocr Pract. 2007 Nov-Dec; 13(7): 716-20. (UPSIT)
2011
- Koenigkam-Santos M, Santos AC, Versiani BR, Diniz PR, Junior JE, de Castro M. Quantitative Magnetic Resonance Imaging Evaluation of the Olfactory System in Kallmann Syndrome: Correlation with a Clinical Smell Test. Neuroendocrinology. 2011; 94(3): 209-17. (UPSIT)
2012
- Lewkowitz-Shpuntoff HM, Hughes VA, Plummer L, Au MG, Doty RL, Seminara SB, Chan YM, Pitteloud N, Crowley WF Jr, Balasubramanian R. Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications. J Clin Endocrinol Metab. 2012 Jan; 97(1): E136-44. (UPSIT)
2013
- Jagtap VS, Sarathi V, Lila AR, Nair S, Bukan A, Sankhe SS, Shivane V, Bandgar T, Menon P, Shah NS. An Objective Olfactory Evaluation and Its Correlation with MRI Findings in Asian Indian Patients with Idiopathic Hypogonadotropic Hypogonadism. Endocr Pract. 2013 Mar 19:1-18. (UPSIT)
- Della Valle E, Vezzani S, Rochira V, Granata AR, Madeo B, Genovese E, Pignatti E, Marino M, Carani C, Simoni M. Prevalence of olfactory and other developmental anomalies in patients with central hypogonadotropic hypogonadism. Front Endocrinol (Lausanne). 2013 Jun 7;4:70. doi: 10.3389/fendo.2013.00070. eCollection 2013 (BSIT)
2014
- Fornazieri MA, Borges BB, Bezerra TF, Pinna Fde R, Voegels RL. Main causes and diagnostic evaluation in patients with primary complaint of olfactory disturbances. Braz J Otorhinolaryngol. May-Jun 2014;80(3):202-7. (UPSIT)
2024
- Zouaghi Y, Choudhary AM, Irshad S, Adamo M, Rehman KU, Fatima A, Shahid M, Najmi N, De Azevedo Correa F, Habibi I, Boizot A, Niederländer NJ, Ansar M, Santoni F, Acierno J, Pitteloud N. Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. BMC Genomics. 2024 Aug 14;25(1):787. doi: 10.1186/s12864-024-10598-3. PMID: 39143522; PMCID: PMC11325732. (UPSIT)