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kw.\*:("restrictive cardiomyopathy")

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Results 1 to 25 of 49

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Magnetic resonance imaging of primary cardiomyopathiesSOLER, Rafaela; RODRIGUEZ, Esther; REMUINAN, Carmen et al.Journal of computer assisted tomography. 2003, Vol 27, Num 5, pp 724-734, issn 0363-8715, 11 p.Article

Outcomes of Restrictive Cardiomyopathy in Childhood and the Influence of Phenotype: A Report From the Pediatric Cardiomyopathy RegistryWEBBER, Steven A; LIPSHULTZ, Steven E; KANTOR, Paul F et al.Circulation (New York, N.Y.). 2012, Vol 126, Num 10, pp 1237-1244, issn 0009-7322, 8 p.Article

Deletion in TNNI3 gene is associated with restrictive cardiomyopathyKOSTAREVA, Anna; GUDKOVA, Alexandra; SJÖBERG, Gunnar et al.International journal of cardiology. 2009, Vol 131, Num 3, pp 410-412, issn 0167-5273, 3 p.Article

Titin Mutation in Familial Restrictive CardiomyopathyPELED, Yael; GRAMLICH, Michael; GEIGER, Dan et al.International journal of cardiology. 2014, Vol 171, Num 1, pp 24-30, issn 0167-5273, 7 p.Article

Cardiac amyloidosisSCHMIDHEINY, Pascal; HESS, Otto M.Heart and metabolism. 2010, Num 49, pp 33-36, issn 1566-0338, 4 p.Article

An unusual case of cardiac amyloidosisGARIBALDI, Brian; ZAAS, David.Journal of general internal medicine. 2007, Vol 22, Num 7, pp 1047-1052, issn 0884-8734, 6 p.Article

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiologyMENON, S. C; MICHELS, V. V; PELLIKKA, P. A et al.Clinical genetics. 2008, Vol 74, Num 5, pp 445-454, issn 0009-9163, 10 p.Article

Pediatric restrictive cardiomyopathy associated with a mutation in β-myosin heavy chainWARE, S. M; QUINN, M. E; BOLLARD, E. T et al.Clinical genetics. 2008, Vol 73, Num 2, pp 165-170, issn 0009-9163, 6 p.Article

Diagnosis of constrictive pericarditis by quantitative tissue Doppler imagingLU, Xiao-Fang; WANG, Xin-Fang; CHENG, Tsung O et al.International journal of cardiology. 2009, Vol 137, Num 1, pp 22-28, issn 0167-5273, 7 p.Article

Impaired contractile function and calcium handling in hearts of cardiac-specific calcineurin b1-deficient miceSCHAEFFER, Paul J; DESANTIAGO, Jaime; KELLY, Daniel P et al.American journal of physiology. Heart and circulatory physiology. 2009, Vol 66, Num 4, issn 0363-6135, H1263-H1273Article

Coffin―Lowry Syndrome and Left Ventricular Noncompaction Cardiomyopathy With a Restrictive PatternMARTINEZ, Hugo R; NIU, Mary C; SUTTON, V. Reid et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3030-3034, issn 1552-4825, 5 p.Article

Furthering the Link Between the Sarcomere and Primary Cardiomyopathies: Restrictive Cardiomyopathy Associated With Multiple Mutations in Genes Previously Associated With Hypertrophic or Dilated CardiomyopathyCALESHU, Colleen; SAKHUJA, Rahul; NUSSBAUM, Robert L et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 9, pp 2229-2235, issn 1552-4825, 7 p.Article

Misleading terms in Anderson-Fabry diseaseWEIDEMANN, F; STROTMANN, J. M; BREUNIG, F et al.European journal of clinical investigation. 2008, Vol 38, Num 3, pp 191-196, issn 0014-2972, 6 p.Article

Extracardiac medical and neuromuscular implications in restrictive cardiomyopathySTOLLBERGER, Claudia; FINSTERER, Josef.Clinical cardiology (Mahwah, NJ). 2007, Vol 30, Num 8, pp 375-380, issn 0160-9289, 6 p.Article

Disturbance in Z-Disk Mechanosensitive Proteins Induced by a Persistent Mutant Myopalladin Causes Familial Restrictive CardiomyopathyHUBY, Anne-Cecile; MENDSAIKHAN, Uzmee; ROBBINS, Jeffrey et al.Journal of the American College of Cardiology. 2014, Vol 64, Num 25, pp 2765-2776, issn 0735-1097, 12 p.Article

Cardiomyopathies restrictives de l'enfant : bilan et approche thérapeutiqueBONNET, Damien.Archives des maladies du coeur et des vaisseaux. Pratique. 2007, Num 158, issn 1261-694X, 12Article

Familial Restrictive Cardiomyopathy With 12 Affected Family MembersDANESHVAR, Daniel A; KEDIA, Gautam; FISHBEIN, Michael C et al.The American journal of cardiology. 2012, Vol 109, Num 3, pp 445-447, issn 0002-9149, 3 p.Article

Restrictive cardiomyopathy in India : the story of a vanishing mysterySIVASANKARAN, S.Heart (London 1996). 2009, Vol 95, Num 1, pp 9-14, issn 1355-6037, 6 p.Article

Aspects of a neglected tropical cardiomyopathy : Endomyocardial fibrosisMARIJON, Eloi.Archives of cardiovascular diseases. 2008, Vol 101, Num 11-12, pp 801-802, issn 1875-2136, 2 p.Article

LE CAS CLINIQUE DU MOIS: Péricardite constrictive = CONSTRICTIVE PERICARDITIS: CASE REPORT AND REVIEWJOHNEN, J; RADERMECKER, M. A; DEFRAIGNE, J. O et al.RMLG. Revue médicale de Liège. 2012, Vol 67, Num 3, pp 107-112, issn 0370-629X, 6 p.Article

Cardiac amyloidosis associated with a novel transthyretin aspartic acid-18 glutamic acid de novo mutationIMAMURA, Takuroh; NAKAZATO, Masamitsu; MATSUO, Takeshi et al.Circulation journal. 2003, Vol 67, Num 11, pp 965-968, issn 1346-9843, 4 p.Article

Restrictive Cardiomyopathy Secondary to Hydroxychloroquine TherapyMANOHAR, Vinayak A; MODER, Kevin G; EDWARDS, William D et al.Journal of rheumatology. 2009, Vol 36, Num 2, pp 440-441, issn 0315-162X, 2 p.Article

Le cas clinique du mois : Péricardite constrictive à péricarde macroscopiquement normal : à propos d'un cas = Constrictive pericarditis with a macroscopically normal pericardiumHOFFER, E; MATERNE, P; LIMET, R et al.RMLG. Revue médicale de Liège. 2007, Vol 62, Num 4, pp 184-187, issn 0370-629X, 4 p.Article

How to manage primary amyloidosisGERTZ, M. A.Leukemia. 2012, Vol 26, Num 2, pp 191-198, issn 0887-6924, 8 p.Article

Factors associated with establishing a causal diagnosis for children with cardiomyopathyCOX, Gerald F; SLEEPER, Lynn A; LOWE, April M et al.Pediatrics (Evanston). 2006, Vol 118, Num 4, pp 1519-1531, issn 0031-4005, 13 p.Article

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