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

Year Number of Results
1976 2
1978 1
1983 1
1986 1
1988 1
1990 1
1994 2
1997 1
2000 1
2005 2
2007 3
2008 1
2009 1
2011 4
2013 3
2014 4
2015 3
2017 1
2018 2
2020 1
2021 3
2022 2
2023 1
2024 1

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38 results

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Page 1
Multiple endocrine neoplasia type 2: A review.
Mathiesen JS, Effraimidis G, Rossing M, Rasmussen ÅK, Hoejberg L, Bastholt L, Godballe C, Oturai P, Feldt-Rasmussen U. Mathiesen JS, et al. Semin Cancer Biol. 2022 Feb;79:163-179. doi: 10.1016/j.semcancer.2021.03.035. Epub 2021 Apr 1. Semin Cancer Biol. 2022. PMID: 33812987 Review.
MEN 2A is associated with medullary thyroid carcinoma (MTC), phaeochromocytoma, primary hyperparathyroidism, cutaneous lichen amyloidosis and Hirschprung's disease and MEN 2B with MTC, phaeochromocytoma, ganglioneuromatosis of the aerodigestive tract, musculoskeletal and o …
MEN 2A is associated with medullary thyroid carcinoma (MTC), phaeochromocytoma, primary hyperparathyroidism, cutaneous lichen amyloidosis an …
Pediatric intestinal motility disorders.
Gfroerer S, Rolle U. Gfroerer S, et al. World J Gastroenterol. 2015 Sep 7;21(33):9683-7. doi: 10.3748/wjg.v21.i33.9683. World J Gastroenterol. 2015. PMID: 26361414 Free PMC article. Review.
This editorial also includes rare causes of pediatric intestinal motility disorders such as hypoganglionosis, dysganglionosis, chronic intestinal pseudo-obstruction and ganglioneuromatosis in multiple endocrine metaplasia. Underlying organic pathologies are rare in pediatr …
This editorial also includes rare causes of pediatric intestinal motility disorders such as hypoganglionosis, dysganglionosis, chronic intes …
Hereditary gastrointestinal polyposis syndromes.
Haggitt RC, Reid BJ. Haggitt RC, et al. Am J Surg Pathol. 1986 Dec;10(12):871-87. doi: 10.1097/00000478-198612000-00006. Am J Surg Pathol. 1986. PMID: 3024515 Review.
The hamartomatous polyposes include Peutz-Jeghers syndrome, familial juvenile polyposis, Cowden's disease, intestinal ganglioneuromatosis, and the Ruvalcaba-Myrhe-Smith syndrome. The incidence of gastrointestinal cancer in patients with Peutz-Jeghers syndrome and familial …
The hamartomatous polyposes include Peutz-Jeghers syndrome, familial juvenile polyposis, Cowden's disease, intestinal ganglioneuromatosis …
Multiple endocrine neoplasia type 2: an overview.
Moline J, Eng C. Moline J, et al. Genet Med. 2011 Sep;13(9):755-64. doi: 10.1097/GIM.0b013e318216cc6d. Genet Med. 2011. PMID: 21552134 Free article. Review.
Individuals with multiple endocrine neoplasia type 2B often have distinct physical features including mucosal neuromas of the lips and tongue, medullated corneal nerve fibers, ganglioneuromatosis of the gastrointestinal tract, distinctive facies with enlarged lips, and a " …
Individuals with multiple endocrine neoplasia type 2B often have distinct physical features including mucosal neuromas of the lips and tongu …
Multiple endocrine neoplasia, type 2b.
Carney JA, Sizemore GW, Hayles AB. Carney JA, et al. Pathobiol Annu. 1978;8:105-53. Pathobiol Annu. 1978. PMID: 364372 Review.
Major portions of the autonomic nervous system, both sympathetic and parasympathetic, nerves and ganglia, exhibit hypertrophy, hyperplasia, and disorder of structure--a group of changes designated ganglioneuromatosis. This may be largely responsible for the striking eye an …
Major portions of the autonomic nervous system, both sympathetic and parasympathetic, nerves and ganglia, exhibit hypertrophy, hyperplasia, …
Classification and diagnostic criteria of variants of Hirschsprung's disease.
Friedmacher F, Puri P. Friedmacher F, et al. Pediatr Surg Int. 2013 Sep;29(9):855-72. doi: 10.1007/s00383-013-3351-3. Pediatr Surg Int. 2013. PMID: 23943250 Review.
Variants of HD include intestinal neuronal dysplasia, intestinal ganglioneuromatosis, isolated hypoganglionosis, immature ganglia, absence of the argyrophil plexus, internal anal sphincter achalasia and congenital smooth muscle cell disorders such as megacystis microcolon …
Variants of HD include intestinal neuronal dysplasia, intestinal ganglioneuromatosis, isolated hypoganglionosis, immature ganglia, ab …
A practical guide for the diagnosis of primary enteric nervous system disorders.
Schäppi MG, Staiano A, Milla PJ, Smith VV, Dias JA, Heuschkel R, Husby S, Mearin ML, Papadopoulou A, Ruemmele FM, Vandenplas Y, Koletzko S. Schäppi MG, et al. J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):677-86. doi: 10.1097/MPG.0b013e3182a8bb50. J Pediatr Gastroenterol Nutr. 2013. PMID: 24177787 Review.
Diagnosis, treatment, and follow-up of medullary thyroid carcinoma: recommendations by the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism.
Maia AL, Siqueira DR, Kulcsar MA, Tincani AJ, Mazeto GM, Maciel LM. Maia AL, et al. Arq Bras Endocrinol Metabol. 2014 Oct;58(7):667-700. doi: 10.1590/0004-2730000003427. Arq Bras Endocrinol Metabol. 2014. PMID: 25372577 English, Portuguese.
CONCLUSIONS: MTC should be suspected in individuals who present with thyroid nodules and family histories of MTC, associations with pheochromocytoma and hyperparathyroidism, and/or typical phenotypic characteristics such as ganglioneuromatosis and Marfanoid habitus. Fine-n …
CONCLUSIONS: MTC should be suspected in individuals who present with thyroid nodules and family histories of MTC, associations with pheochro …
The histopathology of gastrointestinal motility disorders in children.
Feichter S, Meier-Ruge WA, Bruder E. Feichter S, et al. Semin Pediatr Surg. 2009 Nov;18(4):206-11. doi: 10.1053/j.sempedsurg.2009.07.002. Semin Pediatr Surg. 2009. PMID: 19782302 Review.
In intestinal neuronal dysplasia type B, submucous plexus development is disturbed. Immaturity of the enteric nervous system, but also ganglioneuromatosis, can be the underlying cause of chronic constipation. ...
In intestinal neuronal dysplasia type B, submucous plexus development is disturbed. Immaturity of the enteric nervous system, but also ga …
Impact of Early Diagnostic and Therapeutic Interventions and Clinical Course in Children and Adolescents with Multiple Endocrine Neoplasia Types 1 and 2.
Kim JH, Lee Y, Hwang S, Yoon JH, Kim GH, Yoo HW, Choi JH. Kim JH, et al. Exp Clin Endocrinol Diabetes. 2024 Jan;132(1):39-46. doi: 10.1055/a-2212-7536. Epub 2023 Nov 16. Exp Clin Endocrinol Diabetes. 2024. PMID: 37973156
Subsequently, he underwent a subtotal colectomy because of bowel perforation and submucosal ganglioneuromatosis at 18 years of age. CONCLUSION: This study described the relatively long clinical course of pediatric MEN with a mean follow-up duration of 7.53.8 years. ...
Subsequently, he underwent a subtotal colectomy because of bowel perforation and submucosal ganglioneuromatosis at 18 years of age. C …
38 results