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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1978 1
1988 2
1992 2
1993 1
1994 1
1998 2
1999 1
2000 3
2003 4
2004 2
2005 2
2006 2
2007 2
2008 2
2009 3
2010 4
2011 4
2012 4
2013 1
2014 3
2015 5
2016 9
2017 5
2018 3
2019 8
2020 3
2021 7
2022 6
2023 1

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81 results

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The following term was not found in PubMed: pain-hypohidrosis
Page 1
The role of steroid hormones in the sexual differentiation of the human brain.
Bakker J. Bakker J. J Neuroendocrinol. 2022 Feb;34(2):e13050. doi: 10.1111/jne.13050. Epub 2021 Oct 27. J Neuroendocrinol. 2022. PMID: 34708466 Free article. Review.
Both clinical and neuroimaging data obtained in patients with altered androgen levels/actions (i.e., congenital adrenal hyperplasia or complete androgen insensitivity syndrome [CAIS]), point to an important role of (prenatal) androgens in inducing typical mal …
Both clinical and neuroimaging data obtained in patients with altered androgen levels/actions (i.e., congenital adrenal hyperplasia o …
Gender identity disorder (GID) in adolescents and adults with differences of sex development (DSD): A systematic review and meta-analysis.
Babu R, Shah U. Babu R, et al. J Pediatr Urol. 2021 Feb;17(1):39-47. doi: 10.1016/j.jpurol.2020.11.017. Epub 2020 Nov 12. J Pediatr Urol. 2021. PMID: 33246831 Review.
METHODS: Pubmed/Index medicus were searched for "intersex" [All fields] OR "disorders of sexual differentiation AND "gender identity disorder OR gender dysphoria" [MeSH] for articles published between 2005 and 2020. Typical diagnoses included were congenital adrenal hyperp …
METHODS: Pubmed/Index medicus were searched for "intersex" [All fields] OR "disorders of sexual differentiation AND "gender identity disorde …
Congenital corneal anesthesia.
Ramaesh K, Stokes J, Henry E, Dutton GN, Dhillon B. Ramaesh K, et al. Surv Ophthalmol. 2007 Jan-Feb;52(1):50-60. doi: 10.1016/j.survophthal.2006.10.004. Surv Ophthalmol. 2007. PMID: 17212990 Review.
Congenital corneal anesthesia is a rare clinical entity that poses a diagnostic dilemma, particularly in the pediatric age group. ...The sensory deficit may occur as an isolated abnormality, as part of a complex neurological syndrome, or it may occur in association …
Congenital corneal anesthesia is a rare clinical entity that poses a diagnostic dilemma, particularly in the pediatric age group. ... …
[Congenital insensitivity to pain].
Danziger N, Willer JC. Danziger N, et al. Rev Neurol (Paris). 2009 Feb;165(2):129-36. doi: 10.1016/j.neurol.2008.05.003. Epub 2008 Jul 9. Rev Neurol (Paris). 2009. PMID: 18808773 Review. French.
Congenital insensitivity to pain (CIP) is a rare syndrome with various clinical expressions, characterized by a dramatic impairment of pain perception since birth. ...This radical impairment of nociception mirrors the hereditary pain syndromes associat …
Congenital insensitivity to pain (CIP) is a rare syndrome with various clinical expressions, characterized by a dramati …
Painful and painless channelopathies.
Bennett DL, Woods CG. Bennett DL, et al. Lancet Neurol. 2014 Jun;13(6):587-99. doi: 10.1016/S1474-4422(14)70024-9. Epub 2014 May 6. Lancet Neurol. 2014. PMID: 24813307 Review.
For example, the voltage-gated sodium ion channel Nav1.7 is expressed selectively in sensory and autonomic neurons; inactivating mutations in SCN9A, which encodes Nav1.7, result in congenital insensitivity to pain, whereas gain-of-function mutations in this gene pro …
For example, the voltage-gated sodium ion channel Nav1.7 is expressed selectively in sensory and autonomic neurons; inactivating mutations i …
Congenital disorders of estrogen biosynthesis and action.
Fukami M, Ogata T. Fukami M, et al. Best Pract Res Clin Endocrinol Metab. 2022 Jan;36(1):101580. doi: 10.1016/j.beem.2021.101580. Epub 2021 Sep 13. Best Pract Res Clin Endocrinol Metab. 2022. PMID: 34538723 Review.
Germline loss- and gain-of-function variants in CYP19A1, the gene encoding aromatase, lead to aromatase deficiency and aromatase excess syndrome, respectively. Germline loss-of-function variants in ESR1, the gene encoding estrogen receptor alpha, are known to cause of estr …
Germline loss- and gain-of-function variants in CYP19A1, the gene encoding aromatase, lead to aromatase deficiency and aromatase excess s …
Inherited autonomic neuropathies.
Axelrod FB, Hilz MJ. Axelrod FB, et al. Semin Neurol. 2003 Dec;23(4):381-90. doi: 10.1055/s-2004-817722. Semin Neurol. 2003. PMID: 15088259 Review.
The best known and most intensively studied of the HSANs are familial dysautonomia (Riley-Day syndrome or HSAN type III) and congenital insensitivity to pain with anhidrosis (HSAN type IV). ...
The best known and most intensively studied of the HSANs are familial dysautonomia (Riley-Day syndrome or HSAN type III) and conge …
Sodium channelopathies and pain.
Lampert A, O'Reilly AO, Reeh P, Leffler A. Lampert A, et al. Pflugers Arch. 2010 Jul;460(2):249-63. doi: 10.1007/s00424-009-0779-3. Epub 2010 Jan 26. Pflugers Arch. 2010. PMID: 20101409 Review.
Several mutations in the SCN9A gene encoding for Nav1.7 have been identified as important cellular substrates for different heritable pain syndromes. This review aims to cover recent progress on our understanding of how biophysical properties of mutant Nav1.7 translate int …
Several mutations in the SCN9A gene encoding for Nav1.7 have been identified as important cellular substrates for different heritable pain …
Breast Cancer and Major Deviations of Genetic and Gender-related Structures and Function.
Coelingh Bennink HJT, Egberts JFM, Mol JA, Roes KCB, van Diest PJ. Coelingh Bennink HJT, et al. J Clin Endocrinol Metab. 2020 Sep 1;105(9):dgaa404. doi: 10.1210/clinem/dgaa404. J Clin Endocrinol Metab. 2020. PMID: 32594127 Review.
We have searched the literature for information on the risk of breast cancer (BC) in relation to gender, breast development, and gonadal function in the following 8 populations: 1) females with the Turner syndrome (45, XO); 2) females and males with congenital hypog …
We have searched the literature for information on the risk of breast cancer (BC) in relation to gender, breast development, and gonadal fun …
Disorders of Sexual Development in Adult Women.
Gomez-Lobo V, Amies Oelschlager AM; North American Society for Pediatric and Adolescent Gynecology. Gomez-Lobo V, et al. Obstet Gynecol. 2016 Nov;128(5):1162-1173. doi: 10.1097/AOG.0000000000001672. Obstet Gynecol. 2016. PMID: 27741188 Free PMC article. Review.
Three of the most common differences of sex development conditions include congenital adrenal hyperplasia, complete androgen insensitivity, and Turner syndrome. ...Women with Turner syndrome often have congenital anomalies and autoimmune disorde …
Three of the most common differences of sex development conditions include congenital adrenal hyperplasia, complete androgen insen …
81 results