|
10 "Oldest" Classic References 50261. McKusick,VA (1962): Heritable disorders of connective tissue. Trans. Stud. Coll. Physicians Phila. 29(3), 112-126. 52909. Schimke,RN; McKusick,VA; Pollack,AD (1965): Homocystinuria simulating the Marfan syndrome. Trans. Assoc. Am. Physicians 78, 60-72. 5286. Simpson,CF; Kling,JM; Palmer,RF (1970): Beta-aminoproprionitrile-induced dissecting aneurysms of turkeys: Treatment with propranolol. Toxico. Appl. Pharmacol. 16, 143-153. 1750. Beals,RK; Hecht,F (1971): Congenital contractural arachnodactyly: heritable disorder of connective tissue. J. Bone Joint Surg. [Am] 53(A), 987-993. 2267. Dignan,PSJ; Kreines,K; Soukup,S; Warkany,J (1972): Arachnodactyly (Marfan's syndrome) with XYY karyotype. Am. J. Dis. Child. 124, 266-270. 1751. Lipson,EH; Viseskul,C; Herrmann,J (1974): The clinical spectrum of congenital contractural arachnodactyly: a case with congenital heart disease. Z. Kinderheilkd. 118, 1-8. 676. Brown,OR; DeMots,H; Kloster,FE; Roberts,A; Menashe,VD; Beals,RK (1975): Aortic Root Dilatation and Mitral Valve Prolapse in Marfan's Syndrome. An Echocardiographic Study. Circulation 52, 651-657. 3426. Swensson,RE; Linnebur,AC; Paster,SB (1975): Striking aortic root dilation in a patient with the Larsen Syndrome. J. Pediatr. 86(6), 914-915. 60410. Skovby,F; McKusick,VA (1977): Estrogen treatment of tall stature in girls with the Marfan syndrome. In: Natural History of Specific Birth Defects. Vol. 3. (Eds: Bergsma,D; Lowry,RB) (Series Ed: Bergsma,D. Birth Defects: Original Article Series, Volume 13, No. 3C.) Alan R. Liss, Inc., New York, 155-161. 5043. Minor,RR (1980): Collagen metabolism. Am. J. Pathol. 98(1), 227-280. Files Deleted - Restart with recent 10 ... 21769. Moeller,JL (1996): Contraindications to Athletic Participation. Spinal, Systemic, Dermatologic, Paried-Organ, and Other Issues. The Physician and Sportsmedicine 24(9), 57-70. 21768. Moeller,JL (1996): Contraindications to Athletic Participation. Cardiac, Respiratory, and Central Nervous System Conditions. The Physician and Sportsmedicine 24(8), 47-58. 21684. Isherwood,DM (1996): Homocystinuria. Br. Med. J. 313, 1025-1026. 21013. Milewicz,DM; Grossfield,J; Cao,S-N; Kielty,C; Covitz,W; Jewett,T (1995): A mutation in FBN1 disrupts profibrilin processing and results in isolated skeletal features of the Marfan syndrome. J. Clin. Invest. 95, 2373-2378. 21007. Kosztolanyi,G; Weisenbach,J; Mehes,K (1995): Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation. Am. J. Med. Genet. 58, 213-216. 21777. Cheitlin,MD; Douglas,PS; Parmley,WW (1994): Task Force 2: Acquired Valvular Heart Disease. J. Am. Coll. Cardiol. 24(4), 874-899. 21776. Graham,TP Jr; Bricker,JT; James,FW; Strong,WB (1994): Task Force 1: Congenital Heart Disease. J. Am. Coll. Cardiol. 24(4), 867-873. 21775. Mitchell,JH; Haskell,WL; Raven,PB (1994): Classification of Sports. J. Am. Coll. Cardiol. 24(4), 864-866. 21774. Mitten,MJ; Maron,BJ (1994): Legal Considerations that Affect Medical Eligibility for Competitive Athletes with Cardiovascular Abnormalities and Acceptance of Bethesda Conference Recommendations. J. Am. Coll. Cardiol. 24(4), 861-863. 21773. Hutter,AM (1994): Cardiovascular Abnormalities in the Athlete: Role of the Physician. J. Am. Coll. Cardiol. 24(4), 851. |
Marfan Syndrome
