Kallmann syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kallmann syndrome" in English language version.

refsWebsite

Global rank English rank

51nih.gov

4^th place

36doi.org

2^nd place

4worldcat.org

5^th place

4semanticscholar.org

11^th place

8^th place

2medscape.com

719^th place

636^th place

1handle.net

102^nd place

76^th place

1whonamedit.com

2,888^th place

2,730^th place

1rarediseases.org

5,181^st place

3,260^th place

1gutenberg.org

489^th place

377^th place

doi.org

Young, J. (1999-08-01). "Antimullerian Hormone in Patients with Hypogonadotropic Hypogonadism". Journal of Clinical Endocrinology & Metabolism. 84 (8): 2696–2699. doi:10.1210/jcem.84.8.5972. ISSN 0021-972X. PMID 10443662.
Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, Dunkel L, Dwyer AA, Giacobini P, Hardelin JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J (September 2015). "Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment". Nature Reviews. Endocrinology. 11 (9): 547–64. doi:10.1038/nrendo.2015.112. hdl:11567/821921. PMID 26194704.
Garrosa, M. (2024). "Sesquicentenary of the first Chair of Histology in Spain. Aureliano Maestre of San Juan". Actualidad Medica. 109 (818): 7–8. doi:10.15568/am.2024.818.ed01. ISSN 2605-2083.
Dunkel L, Quinton R (June 2014). "Transition in endocrinology: induction of puberty". European Journal of Endocrinology. 170 (6): R229–39. doi:10.1530/EJE-13-0894. PMID 24836550.
Christiansen, Peter; Skakkebæk, Niels E. (2002). "Pulsatile Gonadotropin-Releasing Hormone Treatment of Men with Idiopathic Hypogonadotropic Hypogonadism". Hormone Research in Paediatrics. 57 (1–2): 32–36. doi:10.1159/000057944. ISSN 1663-2818. PMID 12006717.
Lima Amato LG, Latronico AC, Gontijo Silveira LF (June 2017). "Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism". Endocrinology and Metabolism Clinics of North America. 46 (2): 283–303. doi:10.1016/j.ecl.2017.01.010. PMID 28476224.
Laitinen EM, Vaaralahti K, Tommiska J, Eklund E, Tervaniemi M, Valanne L, Raivio T (June 2011). "Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland". Orphanet Journal of Rare Diseases. 6 (Jun 17): 41. doi:10.1186/1750-1172-6-41. PMC 3143089. PMID 21682876.
Kim SH (December 2015). "Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future". Endocrinology and Metabolism. 30 (4): 456–66. doi:10.3803/EnM.2015.30.4.456. PMC 4722398. PMID 26790381.
Dodé, C.; Hardelin, J.-P. (May 2010). "Clinical genetics of Kallmann syndrome". Annales d'Endocrinologie. 71 (3): 149–157. doi:10.1016/j.ando.2010.02.005. ISSN 0003-4266.
Mitchell AL, Dwyer A, Pitteloud N, Quinton R (July 2011). "Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory". Trends in Endocrinology and Metabolism. 22 (7): 249–58. doi:10.1016/j.tem.2011.03.002. PMID 21511493. S2CID 23578201.
Chopra R, Chander A, Jacob JJ (May 2012). "The eye as a window to rare endocrine disorders". Indian Journal of Endocrinology and Metabolism. 16 (3): 331–8. doi:10.4103/2230-8210.95659. PMC 3354836. PMID 22629495.
Jaffe MJ, Sherins RJ, de Monasterio F (1989). Colour Vision Deficiencies IX. Documenta Ophthalmologica Proceedings Series. Dordrecht: Springer. pp. 201–207. doi:10.1007/978-94-009-2695-0_24. ISBN 9789401077156.
Guo CY, Jones TH, Eastell R (February 1997). "Treatment of isolated hypogonadotropic hypogonadism effect on bone mineral density and bone turnover". The Journal of Clinical Endocrinology and Metabolism. 82 (2): 658–65. doi:10.1210/jcem.82.2.3758. PMID 9024272.
Laitinen EM, Hero M, Vaaralahti K, Tommiska J, Raivio T (August 2012). "Bone mineral density, body composition and bone turnover in patients with congenital hypogonadotropic hypogonadism". International Journal of Andrology. 35 (4): 534–40. doi:10.1111/j.1365-2605.2011.01237.x. PMID 22248317.
Wimalawansa SJ, Razzaque DM, Al-Daghri NM (December 2017). "Calcium and Vitamin D in Human Health: Hype or Real?". The Journal of Steroid Biochemistry and Molecular Biology. Dec 16: 4–14. doi:10.1016/j.jsbmb.2017.12.009. PMID 29258769. S2CID 11467429.
Golds G, Houdek D, Arnason T (2017). "Male Hypogonadism and Osteoporosis: The Effects, Clinical Consequences, and Treatment of Testosterone Deficiency in Bone Health". Int J Endocrinol. 2017: 4602129. doi:10.1155/2017/4602129. PMC 5376477. PMID 28408926.
Layman LC (May 2013). "Clinical genetic testing for Kallmann syndrome". The Journal of Clinical Endocrinology and Metabolism. 98 (5): 1860–2. doi:10.1210/jc.2013-1624. PMC 3644595. PMID 23650337.
Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A (2014). "Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes". Frontiers in Endocrinology. 5 (109): 109. doi:10.3389/fendo.2014.00109. PMC 4088923. PMID 25071724.
Au MG, Crowley WF, Buck CL (October 2011). "Genetic counseling for isolated GnRH deficiency". Molecular and Cellular Endocrinology. 346 (1–2): 102–9. doi:10.1016/j.mce.2011.05.041. PMC 3185214. PMID 21664415.
Teixeira L, Guimiot F, Dodé C, Fallet-Bianco C, Millar RP, Delezoide AL, Hardelin JP (October 2010). "Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions". The Journal of Clinical Investigation. 120 (10): 3668–72. doi:10.1172/JCI43699. PMC 2947242. PMID 20940512.
Pitteloud N (December 2012). "Managing delayed or altered puberty in boys". BMJ. 345 (Dec 3): e7913. doi:10.1136/bmj.e7913. PMID 23207503. S2CID 5159169.
Young J (March 2012). "Approach to the male patient with congenital hypogonadotropic hypogonadism". The Journal of Clinical Endocrinology and Metabolism. 97 (3): 707–18. doi:10.1210/jc.2011-1664. PMID 22392951.
Quinton R (April 2005). "Adolescent development: advice in ABC of adolescence is potentially misleading". BMJ. 330 (7494): 789, author reply 789. doi:10.1136/bmj.330.7494.789. PMC 555895. PMID 15802728.
Bry-Gauillard H, Trabado S, Bouligand J, Sarfati J, Francou B, Salenave S, Chanson P, Brailly-Tabard S, Guiochon-Mantel A, Young J (May 2010). "Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics". Annales d'Endocrinologie. 71 (3): 158–62. doi:10.1016/j.ando.2010.02.024. PMID 20363464.
Bouvattier C, Maione L, Bouligand J, Dodé C, Guiochon-Mantel A, Young J (October 2011). "Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism". Nature Reviews. Endocrinology. 8 (3): 172–82. doi:10.1038/nrendo.2011.164. PMID 22009162. S2CID 4564169.
Han TS, Bouloux PM (June 2010). "What is the optimal therapy for young males with hypogonadotropic hypogonadism?". Clinical Endocrinology. 72 (6): 731–7. doi:10.1111/j.1365-2265.2009.03746.x. PMID 19912242.
Maione L, Dwyer AA, Francou B, Guiochon-Mantel A, Binart N, Bouligand J, Young J (March 2018). "GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing". European Journal of Endocrinology. 178 (3): R55–R80. doi:10.1530/EJE-17-0749. PMID 29330225.
Sidhoum VF, Chan YM, Lippincott MF, Balasubramanian R, Quinton R, Plummer L, Dwyer A, Pitteloud N, Hayes FJ, Hall JE, Martin KA, Boepple PA, Seminara SB (March 2014). "Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system". The Journal of Clinical Endocrinology and Metabolism. 99 (3): 861–70. doi:10.1210/jc.2013-2809. PMC 3942233. PMID 24423288.
Dwyer AA, Raivio T, Pitteloud N (June 2016). "MANAGEMENT OF ENDOCRINE DISEASE: Reversible hypogonadotropic hypogonadism". European Journal of Endocrinology. 174 (6): R267–74. doi:10.1530/EJE-15-1033. PMID 26792935.
Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A (2014). "Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes". Frontiers in Endocrinology. 5: 109. doi:10.3389/fendo.2014.00109. PMC 4088923. PMID 25071724.
Skorupskaite K, George JT, Anderson RA (2014). "The kisspeptin-GnRH pathway in human reproductive health and disease". Human Reproduction Update. 20 (4): 485–500. doi:10.1093/humupd/dmu009. PMC 4063702. PMID 24615662.
George JT, Seminara SB (November 2012). "Kisspeptin and the hypothalamic control of reproduction: lessons from the human". Endocrinology. 153 (11): 5130–6. doi:10.1210/en.2012-1429. PMC 3473216. PMID 23015291.

dx.doi.org

Young, J. (1999-08-01). "Antimullerian Hormone in Patients with Hypogonadotropic Hypogonadism". Journal of Clinical Endocrinology & Metabolism. 84 (8): 2696–2699. doi:10.1210/jcem.84.8.5972. ISSN 0021-972X. PMID 10443662.
Garrosa, M. (2024). "Sesquicentenary of the first Chair of Histology in Spain. Aureliano Maestre of San Juan". Actualidad Medica. 109 (818): 7–8. doi:10.15568/am.2024.818.ed01. ISSN 2605-2083.
Christiansen, Peter; Skakkebæk, Niels E. (2002). "Pulsatile Gonadotropin-Releasing Hormone Treatment of Men with Idiopathic Hypogonadotropic Hypogonadism". Hormone Research in Paediatrics. 57 (1–2): 32–36. doi:10.1159/000057944. ISSN 1663-2818. PMID 12006717.
Dodé, C.; Hardelin, J.-P. (May 2010). "Clinical genetics of Kallmann syndrome". Annales d'Endocrinologie. 71 (3): 149–157. doi:10.1016/j.ando.2010.02.005. ISSN 0003-4266.

gutenberg.org

Krafft-Ebing, R. von (Richard); Chaddock, Charles Gilbert (1893). Psychopathia Sexualis: With Especial Reference to Contrary Sexual Instinct: A Medico-Legal Study.

handle.net

hdl.handle.net

Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, Dunkel L, Dwyer AA, Giacobini P, Hardelin JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J (September 2015). "Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment". Nature Reviews. Endocrinology. 11 (9): 547–64. doi:10.1038/nrendo.2015.112. hdl:11567/821921. PMID 26194704.

medscape.com

Lee PA, Houk CP (August 13, 2012). "The Smallest Kid in School: Evaluating Delayed Puberty". Medscape Pediatrics.

emedicine.medscape.com

Tritos, Nicholas A (October 10, 2016). "Kallmann Syndrome and Idiopathic Hypogonadotropic Hypogonadism: Background, Pathophysiology, Epidemiology". eMedicine. {{cite journal}}: Cite journal requires |journal= (help)

nih.gov

pubmed.ncbi.nlm.nih.gov

Young, J. (1999-08-01). "Antimullerian Hormone in Patients with Hypogonadotropic Hypogonadism". Journal of Clinical Endocrinology & Metabolism. 84 (8): 2696–2699. doi:10.1210/jcem.84.8.5972. ISSN 0021-972X. PMID 10443662.
Balasubramanian R, Crowley WF Jr (2017). "Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency". SourceGeneReviews. PMID 20301509.
Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, Dunkel L, Dwyer AA, Giacobini P, Hardelin JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J (September 2015). "Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment". Nature Reviews. Endocrinology. 11 (9): 547–64. doi:10.1038/nrendo.2015.112. hdl:11567/821921. PMID 26194704.
Dunkel L, Quinton R (June 2014). "Transition in endocrinology: induction of puberty". European Journal of Endocrinology. 170 (6): R229–39. doi:10.1530/EJE-13-0894. PMID 24836550.
Christiansen, Peter; Skakkebæk, Niels E. (2002). "Pulsatile Gonadotropin-Releasing Hormone Treatment of Men with Idiopathic Hypogonadotropic Hypogonadism". Hormone Research in Paediatrics. 57 (1–2): 32–36. doi:10.1159/000057944. ISSN 1663-2818. PMID 12006717.
Lima Amato LG, Latronico AC, Gontijo Silveira LF (June 2017). "Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism". Endocrinology and Metabolism Clinics of North America. 46 (2): 283–303. doi:10.1016/j.ecl.2017.01.010. PMID 28476224.
Laitinen EM, Vaaralahti K, Tommiska J, Eklund E, Tervaniemi M, Valanne L, Raivio T (June 2011). "Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland". Orphanet Journal of Rare Diseases. 6 (Jun 17): 41. doi:10.1186/1750-1172-6-41. PMC 3143089. PMID 21682876.
Kim SH (December 2015). "Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future". Endocrinology and Metabolism. 30 (4): 456–66. doi:10.3803/EnM.2015.30.4.456. PMC 4722398. PMID 26790381.
McCabe MJ, Bancalari RE, Dattani MT (February 2014). "Diagnosis and evaluation of hypogonadism". Pediatric Endocrinology Reviews. 11 Suppl 2 (Feb): 214–29. PMID 24683946.
Mitchell AL, Dwyer A, Pitteloud N, Quinton R (July 2011). "Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory". Trends in Endocrinology and Metabolism. 22 (7): 249–58. doi:10.1016/j.tem.2011.03.002. PMID 21511493. S2CID 23578201.
Chopra R, Chander A, Jacob JJ (May 2012). "The eye as a window to rare endocrine disorders". Indian Journal of Endocrinology and Metabolism. 16 (3): 331–8. doi:10.4103/2230-8210.95659. PMC 3354836. PMID 22629495.
Guo CY, Jones TH, Eastell R (February 1997). "Treatment of isolated hypogonadotropic hypogonadism effect on bone mineral density and bone turnover". The Journal of Clinical Endocrinology and Metabolism. 82 (2): 658–65. doi:10.1210/jcem.82.2.3758. PMID 9024272.
Laitinen EM, Hero M, Vaaralahti K, Tommiska J, Raivio T (August 2012). "Bone mineral density, body composition and bone turnover in patients with congenital hypogonadotropic hypogonadism". International Journal of Andrology. 35 (4): 534–40. doi:10.1111/j.1365-2605.2011.01237.x. PMID 22248317.
Wimalawansa SJ, Razzaque DM, Al-Daghri NM (December 2017). "Calcium and Vitamin D in Human Health: Hype or Real?". The Journal of Steroid Biochemistry and Molecular Biology. Dec 16: 4–14. doi:10.1016/j.jsbmb.2017.12.009. PMID 29258769. S2CID 11467429.
Golds G, Houdek D, Arnason T (2017). "Male Hypogonadism and Osteoporosis: The Effects, Clinical Consequences, and Treatment of Testosterone Deficiency in Bone Health". Int J Endocrinol. 2017: 4602129. doi:10.1155/2017/4602129. PMC 5376477. PMID 28408926.
Layman LC (May 2013). "Clinical genetic testing for Kallmann syndrome". The Journal of Clinical Endocrinology and Metabolism. 98 (5): 1860–2. doi:10.1210/jc.2013-1624. PMC 3644595. PMID 23650337.
Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A (2014). "Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes". Frontiers in Endocrinology. 5 (109): 109. doi:10.3389/fendo.2014.00109. PMC 4088923. PMID 25071724.
Vezzoli V, Duminuco P, Bassi I, Guizzardi F, Persani L, Bonomi M (June 2016). "The complex genetic basis of congenital hypogonadotropic hypogonadism". Minerva Endocrinologica. 41 (2): 223–39. PMID 26934720.
Au MG, Crowley WF, Buck CL (October 2011). "Genetic counseling for isolated GnRH deficiency". Molecular and Cellular Endocrinology. 346 (1–2): 102–9. doi:10.1016/j.mce.2011.05.041. PMC 3185214. PMID 21664415.
Teixeira L, Guimiot F, Dodé C, Fallet-Bianco C, Millar RP, Delezoide AL, Hardelin JP (October 2010). "Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions". The Journal of Clinical Investigation. 120 (10): 3668–72. doi:10.1172/JCI43699. PMC 2947242. PMID 20940512.
Pitteloud N (December 2012). "Managing delayed or altered puberty in boys". BMJ. 345 (Dec 3): e7913. doi:10.1136/bmj.e7913. PMID 23207503. S2CID 5159169.
Young J (March 2012). "Approach to the male patient with congenital hypogonadotropic hypogonadism". The Journal of Clinical Endocrinology and Metabolism. 97 (3): 707–18. doi:10.1210/jc.2011-1664. PMID 22392951.
Quinton R (April 2005). "Adolescent development: advice in ABC of adolescence is potentially misleading". BMJ. 330 (7494): 789, author reply 789. doi:10.1136/bmj.330.7494.789. PMC 555895. PMID 15802728.
Dwyer AA, Jayasena CN, Quinton R (June 2016). "Congenital hypogonadotropic hypogonadism: implications of absent mini-puberty". Minerva Endocrinologica. 41 (2): 188–95. PMID 27213784.
Bry-Gauillard H, Trabado S, Bouligand J, Sarfati J, Francou B, Salenave S, Chanson P, Brailly-Tabard S, Guiochon-Mantel A, Young J (May 2010). "Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics". Annales d'Endocrinologie. 71 (3): 158–62. doi:10.1016/j.ando.2010.02.024. PMID 20363464.
Bouvattier C, Maione L, Bouligand J, Dodé C, Guiochon-Mantel A, Young J (October 2011). "Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism". Nature Reviews. Endocrinology. 8 (3): 172–82. doi:10.1038/nrendo.2011.164. PMID 22009162. S2CID 4564169.
Han TS, Bouloux PM (June 2010). "What is the optimal therapy for young males with hypogonadotropic hypogonadism?". Clinical Endocrinology. 72 (6): 731–7. doi:10.1111/j.1365-2265.2009.03746.x. PMID 19912242.
Maione L, Dwyer AA, Francou B, Guiochon-Mantel A, Binart N, Bouligand J, Young J (March 2018). "GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing". European Journal of Endocrinology. 178 (3): R55–R80. doi:10.1530/EJE-17-0749. PMID 29330225.
Sidhoum VF, Chan YM, Lippincott MF, Balasubramanian R, Quinton R, Plummer L, Dwyer A, Pitteloud N, Hayes FJ, Hall JE, Martin KA, Boepple PA, Seminara SB (March 2014). "Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system". The Journal of Clinical Endocrinology and Metabolism. 99 (3): 861–70. doi:10.1210/jc.2013-2809. PMC 3942233. PMID 24423288.
Dwyer AA, Raivio T, Pitteloud N (June 2016). "MANAGEMENT OF ENDOCRINE DISEASE: Reversible hypogonadotropic hypogonadism". European Journal of Endocrinology. 174 (6): R267–74. doi:10.1530/EJE-15-1033. PMID 26792935.
Balasubramanian R, Crowley WF (March 2, 2017). "Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency". GeneReviews. University of Washington, Seattle. PMID 20301509.
De Morsier G, Gauthier G (November 1963). "[Olfacto-Genital Dysplasia]". Pathologie et Biologie. 11: 1267–72. PMID 14099201.
Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A (2014). "Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes". Frontiers in Endocrinology. 5: 109. doi:10.3389/fendo.2014.00109. PMC 4088923. PMID 25071724.
Skorupskaite K, George JT, Anderson RA (2014). "The kisspeptin-GnRH pathway in human reproductive health and disease". Human Reproduction Update. 20 (4): 485–500. doi:10.1093/humupd/dmu009. PMC 4063702. PMID 24615662.
George JT, Seminara SB (November 2012). "Kisspeptin and the hypothalamic control of reproduction: lessons from the human". Endocrinology. 153 (11): 5130–6. doi:10.1210/en.2012-1429. PMC 3473216. PMID 23015291.

ncbi.nlm.nih.gov

Laitinen EM, Vaaralahti K, Tommiska J, Eklund E, Tervaniemi M, Valanne L, Raivio T (June 2011). "Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland". Orphanet Journal of Rare Diseases. 6 (Jun 17): 41. doi:10.1186/1750-1172-6-41. PMC 3143089. PMID 21682876.
Kim SH (December 2015). "Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future". Endocrinology and Metabolism. 30 (4): 456–66. doi:10.3803/EnM.2015.30.4.456. PMC 4722398. PMID 26790381.
Chopra R, Chander A, Jacob JJ (May 2012). "The eye as a window to rare endocrine disorders". Indian Journal of Endocrinology and Metabolism. 16 (3): 331–8. doi:10.4103/2230-8210.95659. PMC 3354836. PMID 22629495.
Golds G, Houdek D, Arnason T (2017). "Male Hypogonadism and Osteoporosis: The Effects, Clinical Consequences, and Treatment of Testosterone Deficiency in Bone Health". Int J Endocrinol. 2017: 4602129. doi:10.1155/2017/4602129. PMC 5376477. PMID 28408926.
Layman LC (May 2013). "Clinical genetic testing for Kallmann syndrome". The Journal of Clinical Endocrinology and Metabolism. 98 (5): 1860–2. doi:10.1210/jc.2013-1624. PMC 3644595. PMID 23650337.
Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A (2014). "Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes". Frontiers in Endocrinology. 5 (109): 109. doi:10.3389/fendo.2014.00109. PMC 4088923. PMID 25071724.
Au MG, Crowley WF, Buck CL (October 2011). "Genetic counseling for isolated GnRH deficiency". Molecular and Cellular Endocrinology. 346 (1–2): 102–9. doi:10.1016/j.mce.2011.05.041. PMC 3185214. PMID 21664415.
Teixeira L, Guimiot F, Dodé C, Fallet-Bianco C, Millar RP, Delezoide AL, Hardelin JP (October 2010). "Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions". The Journal of Clinical Investigation. 120 (10): 3668–72. doi:10.1172/JCI43699. PMC 2947242. PMID 20940512.
Quinton R (April 2005). "Adolescent development: advice in ABC of adolescence is potentially misleading". BMJ. 330 (7494): 789, author reply 789. doi:10.1136/bmj.330.7494.789. PMC 555895. PMID 15802728.
Sidhoum VF, Chan YM, Lippincott MF, Balasubramanian R, Quinton R, Plummer L, Dwyer A, Pitteloud N, Hayes FJ, Hall JE, Martin KA, Boepple PA, Seminara SB (March 2014). "Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system". The Journal of Clinical Endocrinology and Metabolism. 99 (3): 861–70. doi:10.1210/jc.2013-2809. PMC 3942233. PMID 24423288.
Balasubramanian R, Crowley WF (March 2, 2017). "Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency". GeneReviews. University of Washington, Seattle. PMID 20301509.
Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A (2014). "Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes". Frontiers in Endocrinology. 5: 109. doi:10.3389/fendo.2014.00109. PMC 4088923. PMID 25071724.
Skorupskaite K, George JT, Anderson RA (2014). "The kisspeptin-GnRH pathway in human reproductive health and disease". Human Reproduction Update. 20 (4): 485–500. doi:10.1093/humupd/dmu009. PMC 4063702. PMID 24615662.
George JT, Seminara SB (November 2012). "Kisspeptin and the hypothalamic control of reproduction: lessons from the human". Endocrinology. 153 (11): 5130–6. doi:10.1210/en.2012-1429. PMC 3473216. PMID 23015291.

ghr.nlm.nih.gov

"Kallmann syndrome". Genetics Home Reference. US Library of Medicine. National Institutes for Health. Genetic and Rare Diseases Information. June 26, 2016. Retrieved December 17, 2017.
"Kallmann syndrome". National Institutes for Health. US Library of Medicine. Genetics Home Reference. December 2017. Retrieved December 17, 2017.

rarediseases.org

"Kallmann syndrome". Rare Diseases. National Organisation for Rare Disorders (NORD). 2012. Retrieved December 16, 2017.

semanticscholar.org

api.semanticscholar.org

Mitchell AL, Dwyer A, Pitteloud N, Quinton R (July 2011). "Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory". Trends in Endocrinology and Metabolism. 22 (7): 249–58. doi:10.1016/j.tem.2011.03.002. PMID 21511493. S2CID 23578201.
Wimalawansa SJ, Razzaque DM, Al-Daghri NM (December 2017). "Calcium and Vitamin D in Human Health: Hype or Real?". The Journal of Steroid Biochemistry and Molecular Biology. Dec 16: 4–14. doi:10.1016/j.jsbmb.2017.12.009. PMID 29258769. S2CID 11467429.
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