Below are the most recent publications written about "Hypertrophy" by people in Profiles.
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Robbins J, Halegoua-DeMarzio D, Basu Mallick A, Vijayvergia N, Ganetzky R, Lavu H, Giri VN, Miller J, Maley W, Shah AP, DiMeglio M, Ambelil M, Yu R, Sato T, Lefler DS. Liver Transplantation in a Woman with Mahvash Disease. N Engl J Med. 2023 Nov 23; 389(21):1972-1978.
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Paul RW, Sheridan S, Reuther KE, Kelly JD, Thomas SJ. The Contribution of Posterior Capsule Hypertrophy to Soft Tissue Glenohumeral Internal Rotation Deficit in Healthy Pitchers. Am J Sports Med. 2022 Feb; 50(2):341-346.
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Charleston L, Cooper W. An Update on Idiopathic Hypertrophic Cranial Pachymeningitis for the Headache Practitioner. Curr Pain Headache Rep. 2020 Aug 17; 24(10):57.
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Gopal AD, Kim JM, Shields CL. Concurrent solitary and multifocal congenital hypertrophy of the retinal pigment epithelium in a single eye. Indian J Ophthalmol. 2020 07; 68(7):1454.
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Pefkianaki M, Mashayekhi A, Shields JA, Shields CL. Congenital Hypertrophy of Retinal Pigment Epithelium With Overlying Thin Adenoma. Retina. 2017 06; 37(6):e69-e70.
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Hwang MS, Salapatas AM, Yalamanchali S, Joseph NJ, Friedman M. Factors associated with hypertrophy of the lingual tonsils. Otolaryngol Head Neck Surg. 2015 May; 152(5):851-5.
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Friedman M, Yalamanchali S, Gorelick G, Joseph NJ, Hwang MS. A standardized lingual tonsil grading system: interexaminer agreement. Otolaryngol Head Neck Surg. 2015 Apr; 152(4):667-72.
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Ramirez-Correa GA, Frazier AH, Zhu G, Zhang P, Rappold T, Kooij V, Bedja D, Snyder GA, Lugo-Fagundo NS, Hariharan R, Li Y, Shen X, Gao WD, Cingolani OH, Takimoto E, Foster DB, Murphy AM. Cardiac troponin I Pro82Ser variant induces diastolic dysfunction, blunts ?-adrenergic response, and impairs myofilament cooperativity. J Appl Physiol (1985). 2015 Jan 15; 118(2):212-23.
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Tsuda T, Dunn S, Radtke W. Acquired discrete subaortic stenosis in solid organ transplant recipients. Pediatr Transplant. 2014 Aug; 18(5):E161-4.
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Michot C, Le Goff C, Mahaut C, Afenjar A, Brooks AS, Campeau PM, Destree A, Di Rocco M, Donnai D, Hennekam R, Heron D, Jacquemont S, Kannu P, Lin AE, Manouvrier-Hanu S, Mansour S, Marlin S, McGowan R, Murphy H, Raas-Rothschild A, Rio M, Simon M, Stolte-Dijkstra I, Stone JR, Sznajer Y, Tolmie J, Touraine R, van den Ende J, Van der Aa N, van Essen T, Verloes A, Munnich A, Cormier-Daire V. Myhre and LAPS syndromes: clinical and molecular review of 32 patients. Eur J Hum Genet. 2014 Nov; 22(11):1272-7.