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1980 1
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1998 1
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2000 2
2001 1
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2008 3
2009 4
2010 1
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56 results

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Page 1
The neurofibromatosis-Noonan syndrome.
Opitz JM, Weaver DD. Opitz JM, et al. Am J Med Genet. 1985 Jul;21(3):477-90. doi: 10.1002/ajmg.1320210310. Am J Med Genet. 1985. PMID: 3927726 No abstract available.
Multidetector computed tomography-guided percutaneous transluminal septal myocardial ablation in a Noonan syndrome patient with hypertrophic obstructive cardiomyopathy.
Maekawa Y, Jinzaki M, Tsuruta H, Yamada Y, Kishino Y, Kawakami T, Hayashida K, Yuasa S, Murata M, Kawamura A, Sano M, Kuribayashi S, Fukuda K. Maekawa Y, et al. Int J Cardiol. 2014;172(1):e79-81. doi: 10.1016/j.ijcard.2013.12.045. Epub 2013 Dec 28. Int J Cardiol. 2014. PMID: 24411913 No abstract available.
Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature.
Addissie YA, Kotecha U, Hart RA, Martinez AF, Kruszka P, Muenke M. Addissie YA, et al. Am J Med Genet A. 2015 Nov;167A(11):2657-63. doi: 10.1002/ajmg.a.37259. Epub 2015 Aug 6. Am J Med Genet A. 2015. PMID: 26249544 Review.
Noonan syndrome (NS) is a multiple congenital anomaly syndrome caused by germline mutations in genes coding for components of the Ras-mitogen-activated protein kinase (RAS-MAPK) pathway. ...The inclusion of craniosynostosis as a possible phenotype in KRAS-ass …
Noonan syndrome (NS) is a multiple congenital anomaly syndrome caused by germline mutations in genes coding for compone …
Computed tomography after lymphangiography in the diagnosis of intestinal lymphangiectasia with protein-losing enteropathy in Noonan's syndrome.
Keberle M, Mörk H, Jenett M, Hahn D, Scheurlen M. Keberle M, et al. Eur Radiol. 2000;10(10):1591-3. doi: 10.1007/s003300000384. Eur Radiol. 2000. PMID: 11044930
Noonan's syndrome is a rare congenital disorder that may be associated with abnormalities in the lymphatic drainage. In this case of a 21-year-old man CT after bipedal lymphangiography confirmed the diagnosis of intestinal lymphangiectasy causing protein-losing ente …
Noonan's syndrome is a rare congenital disorder that may be associated with abnormalities in the lymphatic drainage. In this c …
Noonan's syndrome with syringomyelia.
Kobayashi I, Aikawa T, Takemiya T, Maruyama S, Takano K. Kobayashi I, et al. Jpn J Psychiatry Neurol. 1986 Mar;40(1):101-4. doi: 10.1111/j.1440-1819.1986.tb01616.x. Jpn J Psychiatry Neurol. 1986. PMID: 3773346
A case of Noonan's syndrome with cervical syringomyelia is presented here representing the second reported instance of such association. ...It could not be determined whether this association between syringomyelia and Noonan's syndrome is related or re …
A case of Noonan's syndrome with cervical syringomyelia is presented here representing the second reported instance of such as …
Cherubism in a patient with Noonan's syndrome.
Addante RR, Breen GH. Addante RR, et al. J Oral Maxillofac Surg. 1996 Feb;54(2):210-3. doi: 10.1016/s0278-2391(96)90449-8. J Oral Maxillofac Surg. 1996. PMID: 8604072 Review. No abstract available.
Rare Congenital Dissecting Thoracic Aortic Aneurysm in a Child with Noonan Syndrome: A Case Report.
Maulana SAA, Alwi SHE, Hashim MS, Rohim RAA. Maulana SAA, et al. Oman Med J. 2023 Nov 30;38(6):e576. doi: 10.5001/omj.2023.66. eCollection 2023 Nov. Oman Med J. 2023. PMID: 38269208 Free PMC article.
We present a rare case of congenital thoracic aortic aneurysm (TAA) complicated with dissection in a nine-year-old girl with Noonan syndrome and atrial septal defect. She presented with rapid breathing and upper respiratory tract symptoms. Chest X-ray …
We present a rare case of congenital thoracic aortic aneurysm (TAA) complicated with dissection in a nine-year-old girl with Noonan …
Multifocal tenosynovial giant cell tumors in a child with Noonan syndrome.
Meyers AB, Awomolo AO, Szabo S. Meyers AB, et al. Pediatr Radiol. 2017 Mar;47(3):361-365. doi: 10.1007/s00247-016-3743-3. Epub 2016 Nov 23. Pediatr Radiol. 2017. PMID: 27878339
The association of Noonan syndrome and giant cell granulomas of the mandible is widely reported. However, Noonan syndrome may also be associated with single or multifocal tenosynovial giant cell tumors, also referred to as pigmented villonodular synovi …
The association of Noonan syndrome and giant cell granulomas of the mandible is widely reported. However, Noonan syn …
Cardiac Arrest in a 31-Year-Old Man With Noonan Syndrome.
Grotti S, Dall'Ara G, Tarantino F, Bachetti C, Ottani F, Galvani M. Grotti S, et al. J Invasive Cardiol. 2019 Feb;31(2):E40. J Invasive Cardiol. 2019. PMID: 30700630 Free article.
A 31-year-old man with Noonan syndrome who suffered an out-of-hospital cardiac arrest presented at our institution with severe postanoxic coma (Glasgow coma scale 3), but normalized electrocardiogram and stable hemodynamics. ...
A 31-year-old man with Noonan syndrome who suffered an out-of-hospital cardiac arrest presented at our institution with severe …
Central xanthoma of the jaw in association with Noonan syndrome.
Olson NJ, Addante RR, de Abreu FB, Memoli VA. Olson NJ, et al. Hum Pathol. 2018 Dec;82:202-205. doi: 10.1016/j.humpath.2018.04.020. Epub 2018 May 1. Hum Pathol. 2018. PMID: 29727697
New evidence supports the hypothesis that central xanthomas are a separate and distinct entity from their extragnathic counterparts. Noonan syndrome (NS) is an autosomal dominant disorder that has been associated with giant cell lesions, which also commonly occur in …
New evidence supports the hypothesis that central xanthomas are a separate and distinct entity from their extragnathic counterparts. Noon …
56 results