R. Lacro

发表

Cardiovascular disease in Noonan syndrome

K. Gauvreau, R. Kucherlapati, A. Roberts, 2014, Archives of Disease in Childhood.

X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects.

K. Jones, R. Lacro, R. Mathias, 1987, American journal of medical genetics.

Increased Vertebral Artery Tortuosity Index Is Associated With Adverse Outcomes in Children and Young Adults With Connective Tissue Disorders

K. Gauvreau, D. Orbach, T. Geva, 2011, Circulation.

Children and Young Adults With Connective Tissue Disorders Increased Vertebral Artery Tortuosity Index Is Associated With Adverse Outcomes in

K. Gauvreau, D. Orbach, T. Geva, 2011 .

Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome

S. B. Wechsler, B. Gelb, F. Trachtenberg, 2016, Pediatric Cardiology.

Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy.

S. B. Wechsler, H. Dietz, L. Guey, 2013, American heart journal.

Echocardiographic methods, quality review, and measurement accuracy in a randomized multicenter clinical trial of Marfan syndrome.

S. Colan, L. Sleeper, L. Guey, 2013, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

Coarctation of the aorta in Turner syndrome: a pathologic study of fetuses with nuchal cystic hygromas, hydrops fetalis, and female genitalia.

K. Benirschke, K. Jones, R. Lacro, 1988, Pediatrics.

Recruitment, retention, and adherence in a clinical trial: The Pediatric Heart Network’s Marfan Trial experience

F. Trachtenberg, V. Pemberton, J. Cnota, 2020, Clinical trials.

Recent Clinical Drug Trials Evidence in Marfan Syndrome and Clinical Implications.

R. Lacro, Michael N. Singh, Michael N Singh, 2016, The Canadian journal of cardiology.

Congenital Heart Disease Increased Vertebral Artery Tortuosity Index Is Associated With Adverse Outcomes in Children and Young Adults With Connective Tissue Disorders

K. Gauvreau, D. Orbach, T. Geva, 2011 .

Ascending aortic dilation in patients with congenital complete heart block.

J. Triedman, C. Berul, E. Walsh, 2008, Heart rhythm.

T. Travison, S. Colan, J. Krischer, 2019, The Journal of pediatrics.

Rationale and design of a randomized clinical trial of beta-blocker therapy (atenolol) versus angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndrome.

S. Colan, J. Saul, R. Devereux, 2007, American heart journal.

Outcomes After Primary Transcatheter Therapy in Infants and Young Children With Severe Bilateral Peripheral Pulmonary Artery Stenosis

K. Gauvreau, J. Lock, D. McElhinney, 2013, Circulation. Cardiovascular interventions.

Clinical and echocardiographic predictors of adverse cardiovascular outcome in childhood marfan syndrome

S. Colan, K. Gauvreau, R. Lacro, 1998 .

New England Congenital Cardiology Association Bicuspid Aortopathy Registry (NECCA BAR): A regional preventive cardiovascular care collaboration

L. Sleeper, E. P. Greenstein, R. Lacro, 2022, Progress in Pediatric Cardiology.

Longitudinal Changes in Segmental Aortic Stiffness Determined by Cardiac Magnetic Resonance in Children and Young Adults With Connective Tissue Disorders (the Marfan, Loeys-Dietz, and Ehlers-Danlos Syndromes, and Nonspecific Connective Tissue Disorders).

K. Gauvreau, R. Lacro, A. Prakash, 2017, The American journal of cardiology.

Renal findings in 40 individuals with Williams syndrome.

B. Pober, V. Mandell, R. Lacro, 1993, American journal of medical genetics.

Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials

S. Neubauer, M. Flather, M. Groenink, 2022, The Lancet.

New autosomal dominant branchio‐oculo‐facial syndrome

J. Opitz, K. Jones, A. Fujimoto, 1987, American journal of medical genetics.

Hemorrhagic infarction and coronary reperfusion.

G. T. Smith, J. Mcnamara, R. Lacro, 1981, The Journal of thoracic and cardiovascular surgery.

Adams-Oliver syndrome associated with cardiovascular malformations.

L. Holmes, M. Westgate, A. Lin, 1998, Clinical dysmorphology.

Three‐Dimensional Mitral Valve Morphology in Children and Young Adults With Marfan Syndrome

M. Nathan, G. Marx, L. Sleeper, 2018, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

W. Chung, J. Priest, W. Pu, 2018, Circulation.

Arterial tortuosity in patients with Filamin A‐ associated vascular aneurysms

S. Robertson, D. Rimoin, S. Morris, 2014, American journal of medical genetics. Part A.

Surgical management of complete atrioventricular septal defect: associations with surgical technique, age, and trisomy 21.

S. Colan, B. McCrindle, L. Sleeper, 2011, The Journal of thoracic and cardiovascular surgery.

Pattern of malformations in the children of women treated with carbamazepine during pregnancy.

K. Jones, J. Adams, R. Lacro, 1989, The New England journal of medicine.

Partial and transitional atrioventricular septal defect outcomes.

S. Colan, L. Sleeper, S. Mital, 2010, The Annals of thoracic surgery.

Pulmonary Artery Hypertension in Formerly Premature Infants With Bronchopulmonary Dysplasia: Clinical Features and Outcomes in the Surfactant Era

D. McElhinney, M. Mullen, R. Lacro, 2007, Pediatrics.

Atenolol versus losartan in children and young adults with Marfan's syndrome.

S. Colan, S. B. Wechsler, H. Dietz, 2014, The New England journal of medicine.

Fetal pulmonary artery diameters and their association with lung hypoplasia and postnatal outcome in congenital diaphragmatic hernia.

J. Smallhorn, L. Hornberger, D. Bohn, 2002, American journal of obstetrics and gynecology.

Surgical interventions for atrioventricular septal defect subtypes: the pediatric heart network experience.

S. Colan, B. McCrindle, L. Sleeper, 2011, The Annals of thoracic surgery.

Sudden death in Williams syndrome: report of ten cases.

C. Morris, H. Hoyme, L. Bird, 1996, The Journal of pediatrics.

Clinical utility of a next generation sequencing panel assay for Marfan and Marfan‐like syndromes featuring aortopathy

J. Stoler, A. Rope, P. Bayrak-Toydemir, 2015, American journal of medical genetics. Part A.

MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus

Ronald Berezney, Kasper Lage, Raymond M. Anchan, 2015, Human molecular genetics.

MATR 3 disruption in human and mouse associated with bicuspid aortic valve , aortic coarctation and patent ductus arteriosus

K. Lage, J. Gusella, C. Morton, 2015 .

Duplication of distal 15q: report of five new cases from two different translocation kindreds.

K. Jones, O. Jones, J. Mascarello, 1987, American journal of medical genetics.

The umbilical cord twist: origin, direction, and relevance.

K. Benirschke, K. Jones, R. Lacro, 1987, American journal of obstetrics and gynecology.

Fetal cardiac dextroposition in the absence of an intrathoracic mass: sign of significant right lung hypoplasia.

J. Smallhorn, D. Chitayat, L. Hornberger, 2000, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Marfan Syndrome and Related Disorders of Fibrillin

R. Lacro, 2000 .

Fetal Echocardiographic Predictors of Morbidity and Mortality in Congenital Diaphragmatic Hernia

L. Hornberger, D. Bohn, G. Ryan, 1999 .

Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations

David T. Miller, D. Milewicz, A. Lin, 2013, American journal of medical genetics. Part A.

Challenges in Echocardiographic Assessment of Mitral Regurgitation in Children After Repair of Atrioventricular Septal Defect

S. Colan, B. McCrindle, L. Sleeper, 2012, Pediatric Cardiology.

Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort

D. Roden, H. Dietz, B. Gelb, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Pattern of Malformations in the Children of Women Treated with Carbamazepine during Pregnancy

Kathleen A. Johnson, K. Jones, R. Lacro, 1990 .

Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaboration

A. Zwinderman, E. Arbustini, S. Neubauer, 2015, American heart journal.

Clinical approach to genetic cardiomyopathy in children.

S. Lipshultz, A. Lin, A. Perez-Atayde, 1996, Circulation.

Genome Sequencing Identifies the Pathogenic Variant Missed by Prior Testing in an Infant with Marfan Syndrome.

A. O’Donnell-Luria, M. Wojcik, W. Tan, 2019, The Journal of pediatrics.

Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2

J. Fish, David T. Miller, J. Graham, 2020, Clinical genetics.

Performant Mutation Identification Using Targeted Next‐Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes

D. Roden, G. Mortier, H. Dietz, 2015, Human mutation.

Lessons learned from a pediatric clinical trial: the Pediatric Heart Network angiotensin-converting enzyme inhibition in mitral regurgitation study.

S. Colan, J. Newburger, L. Sleeper, 2011, American heart journal.

Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome.

D. Roden, H. Dietz, L. Sleeper, 2020, The Journal of pediatrics.

Effect of Losartan or Atenolol on Children and Young Adults with Bicuspid Aortic Valve and Dilated Aorta.

S. Colan, L. Sleeper, R. Lacro, 2020, The American journal of cardiology.

Bicuspid aortic valve and associated aortic dilation in the young

Dionne A. Graham, S. Colan, P. Khairy, 2012, Heart.

Expression of dihydropyridine receptor (Ca2+ channel) and calsequestrin genes in the myocardium of patients with end-stage heart failure.

W Grossman, F J Schoen, F. Schoen, 1992, The Journal of clinical investigation.

Health Supervision for Children and Adolescents With Marfan Syndrome.

B. Tinkle, R. Lacro, L. Burke, 2023, Pediatrics.

Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome.

S. Colan, L. Sleeper, G. Pearson, 2018, The American journal of cardiology.

Segmental Aortic Stiffness in Children and Young Adults With Connective Tissue Disorders: Relationships With Age, Aortic Size, Rate of Dilation, and Surgical Root Replacement

K. Gauvreau, T. Geva, S. Morris, 2015, Circulation.

Cardiovascular malformations: changes in prevalence and birth status, 1972-1990.

L B Holmes, L. Holmes, A. Herring, 1999, American journal of medical genetics.

Dilation of the ascending aorta after balloon valvuloplasty for aortic stenosis during infancy and childhood.

S. Emani, K. Gauvreau, D. McElhinney, 2012, The American journal of cardiology.

Measurement of technical performance in congenital heart surgery: a pilot study.

Kimberlee Gauvreau, John E Mayer, Pedro J del Nido, 2007, The Annals of thoracic surgery.

Abstract 490: Vertebral Artery Tortuosity Index is a Novel Biomarker of Surgery and Aortic Dissection or Rupture in Children and Young Adults: Findings From the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions

K. Eagle, S. Lemaire, D. Milewicz, 2014 .

Potocki–Lupski syndrome: An inherited dup(17)(p11.2p11.2) with hypoplastic left heart

A. Ligon, A. Roberts, R. Lacro, 2011, American journal of medical genetics. Part A.

Randomized trial of atenolol versus losartan in children and young adults with Marfan syndrome

S. Colan, S. B. Wechsler, H. Dietz, 2014 .

Updated consensus guidelines on the management of Phelan–McDermid syndrome

A. Kolevzon, L. Soorya, J. Buxbaum, 2023, American journal of medical genetics. Part A.

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys‐Dietz syndromes

B. Menten, J. Hellemans, A. De Paepe, 2011, Human mutation.

Response to Letters Regarding Article "Segmental Aortic Stiffness in Children and Young Adults With Connective Tissue Disorders: Relationships With Age, Aortic Size, Rate of Dilation, and Surgical Root Replacement".

K. Gauvreau, T. Geva, S. Morris, 2016, Circulation.

The Gorlin syndrome: a genetically determined disorder associated with cardiac tumor.

K. Jones, R. Lacro, 1986, The Journal of thoracic and cardiovascular surgery.

Frequency of Ventricular Arrhythmias and Other Rhythm Abnormalities in Children and Young Adults With the Marfan Syndrome.

B. McCrindle, S. B. Wechsler, L. Sleeper, 2018, The American journal of cardiology.

Heart Size on Chest X-Ray as a Predictor of Cardiac Enlargement by Echocardiography in Children

K. Jenkins, G. Satou, R. Lacro, 2001, Pediatric Cardiology.

Design and rational collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome , based on individual patient data : A report from the Marfan Treatment Trialists ' Collaboration

A. Zwinderman, E. Arbustini, M. Flather, 2015 .

Bicuspid aortic valve and its ascending aortopathy

R. Lacro, E. Dunne, J. Flyer, 2023, Current opinion in pediatrics.

Vertebral artery tortuosity in Turner syndrome: is tortuosity a component of the aortopathy phenotype?

D. Milewicz, S. Maskatia, S. Morris, 2014, Journal of Cardiovascular Magnetic Resonance.

Purification, characterization, and molecular cloning of a 60-kDa phosphoprotein in rabbit skeletal sarcoplasmic reticulum which is an isoform of phosphoglucomutase.

Y. S. Lee, A. Marks, B. Nadal-Ginard, 1992, The Journal of biological chemistry.

Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy.

S. B. Wechsler, L. Guey, S. Paridon, 2013, American heart journal.

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

W. Chung, J. Priest, W. Pu, 2018, Circulation.

Cardiovascular disease in Noonan syndrome

K. Gauvreau, R. Kucherlapati, A. Roberts, 2014, Archives of Disease in Childhood.

Children with Thoracic Aortic Aneurysm: Challenges in Diagnosis and Therapy.

M. Pierpont, R. Lacro, 2015, The Journal of pediatrics.

K. Gauvreau, T. Geva, R. Lacro, 2016, Circulation.

Segmental Aortic Stiffness in Children and Young Adults With Connective Tissue Disorders: Relationships With Age, Aortic Size, Rate of Dilation, and Surgical Root Replacement

K. Gauvreau, T. Geva, R. Lacro, 2015, Circulation.

Segmental Aortic Stiffness in Children and Young Adults With Connective Tissue Disorders Relationships With Age, Aortic Size, Rate of Dilation, and Surgical Root Replacement Pediatric Cardiology

K. Gauvreau, T. Geva, R. Lacro, 2015 .

K. Gauvreau, R. Lacro, A. Prakash, 2017, The American journal of cardiology.

Improved outcome with composite graft versus homograft root replacement for children with aortic root aneurysms.

D. Zurakowski, R. Jonas, B. Mora, 2005, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome.

S. Lemaire, D. Milewicz, S. Oda, 2023, Journal of the American Heart Association.