海量图书期刊资源,随时随地畅享阅读乐趣
Molecular and clinical characterization of a patient with duplication of 1p36.3 and metopic synostosisHA Heilstedt; SK Shapira; AR Gregg; LG Shaffer · 1999
Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal EncephalomyopathyHabibzadeh, Parham; Silawi, Mohammad; Dastsooz, Hassan; Bahramjahan, Shima; Ezzatzadegan Jahromi, Shahrokh; Ostovan, Vahid Reza; Yavarian, Majid; Mofatteh, Mohammad; Faghihi, Mohammad Ali · BMC Gastroenterology · 2020
Molecular and clinical characterization of a Moroccan Cog7 deficient patientBobby G. Ng; Christian Kranz; E.E.O. Hagebeuk; M. Duran; N.G.G.M. Abeling; B. Wuyts; Daniel Ungar; Vladimir Lupashin; C.M. Hartdorff; B.T. Poll-The; Hudson H. Freeze · 2007
Report of a patient and further clinical and molecular characterization of interstitial 4p16.3 microduplicationPalumbo, Orazio; Palumbo, Pietro; Ferri, Emanuela; Riviello, Francesco; Cloroformio, Lea; Carella, Massimo; Di Giacomo, Marilena · Molecular Cytogenetics · 2015
Molecular characterization and clinical features of a patient with an interstitial deletion of 3p25.3-p26.1Cecilia Gunnarsson; Cathrine Foyn Bruun · 2010
Clinical and Molecular Characterization of a Brazilian Patient with Pit-1 DeficiencyArnhold, I.J.P.; Nery, M.; Brown, U.R.; Voss, T.C.; VanderHeyden, T.C.; Addess, M.E.; Hurley, D.L.; Wajchenberg, B.L.; Parks, J.S. · Journal of Pediatric Endocrinology and Metabolism · 1998
Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletionTassano, Elisa; Mirabelli-Badenier, Marisol; Veneselli, Edvige; Puliti, Aldamaria; Lerone, Margherita; Vaccari, Carlotta Maria; Morana, Giovanni; Porta, Simona; Gimelli, Giorgio; Cuoco, Cristina · Molecular Cytogenetics · 2015
Clinical and molecular characterization of the first adult congenital disorder of glycosylation (CDG) type Ic patientLiangwu Sun; Erik A. Eklund; Johan L.K. Van Hove; Hudson H. Freeze; Janet A. Thomas · 2005
Gender-related differences in moral judgmentsM. Fumagalli; R. Ferrucci; F. Mameli; S. Marceglia; S. Mrakic-Sposta; S. Zago; C. Lucchiari; D. Consonni; F. Nordio; G. Pravettoni; S. Cappa; A. Priori · 2010
Genetics of Sudden Cardiac DeathBezzina, C. R.; Lahrouchi, N.; Priori, S. G. · Circulation Research · 2015
Genetic Determinants of Cardiac (Electric) ConductionPriori, S. G. · Circulation Research · 2011
A Clinical Approach to Inherited ArrhythmiasCerrone, M.; Cummings, S.; Alansari, T.; Priori, S. G. · Circulation: Cardiovascular Genetics · 2012
Inherited Arrhythmogenic Diseases: The Complexity Beyond Monogenic DisordersPriori, S. G. · Circulation Research · 2004
Genetics of sudden death: focus on inherited channelopathiesCerrone, M.; Priori, S. G. · European Heart Journal · 2011
Immunofluorescence studies on sera of patients with breast carcinomaElizabeth S. Priori; G. Seman; L. Dmochowski; H. S. Gallager; D. E. Anderson · 1971
Low-frequency subthalamic oscillations increase after deep brain stimulation in Parkinson's diseaseA. Priori; G. Ardolino; S. Marceglia; S. Mrakic-Sposta; M. Locatelli; F. Tamma; L. Rossi; G. Foffani · 2006
Thrombolytic Therapy of Acute StrokeFeske, S. K. · Circulation · 2012
Energy Balance and ObesityHill, J. O.; Wyatt, H. R.; Peters, J. C. · Circulation · 2012
Fluctuation: Does Blood Pressure Variability Matter?Krakoff, L. R. · Circulation · 2012
Sex and Cardiovascular RiskLam, C. S. P.; Little, W. C. · Circulation · 2012
Supravalvular Aortic StenosisWILLIAMS, J. C. P.; BARRATT-BOYES, B. G.; LOWE, J. B. · Circulation · 1961
Transthyretin (TTR) Cardiac AmyloidosisRuberg, F. L.; Berk, J. L. · Circulation · 2012
In Search of Vulnerable PlaqueStone, G. W. · Circulation: Cardiovascular Imaging · 2012
Oral Direct Factor Xa InhibitorsYeh, C. H.; Fredenburgh, J. C.; Weitz, J. I. · Circulation Research · 2012