Fahed, Akl: search on Z-Library

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1

Low-Density Lipoprotein Levels and Not Mutation Status Predict Intima-Media Thickness in Familial Hypercholesterolemia

Fahed, Akl C., Habib, Robert H., Nemer, Georges M., Azar, Sami T., Andary, Rabih R., Arabi, Mariam T., Moubarak, Elie M., Bitar, Fadi F., Haddad, Fady F.

Journal:

Annals of Vascular Surgery

Year:

2014

Language:

english

File:

PDF, 482 KB

english, 2014

2

UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration

Fahed, Akl C., McDonough, Barbara, Gouvion, Cynthia M., Newell, Kathy L., Dure, Leon S., Bebin, Martina, Bick, Alexander G., Seidman, Jonathan G., Harter, Donald H., Seidman, Christine E.

Journal:

Annals of Neurology

Year:

2014

Language:

english

File:

PDF, 228 KB

english, 2014

3

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions

Fahed, Akl C., Wang, Minxian, Homburger, Julian R., Patel, Aniruddh P., Bick, Alexander G., Neben, Cynthia L., Lai, Carmen, Brockman, Deanna, Philippakis, Anthony, Ellinor, Patrick T., Cassa, Christop

Journal:

Nature Communications

Year:

2020

File:

PDF, 926 KB

2020

4

NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

Abou Hassan, Ossama K., Fahed, Akl C., Batrawi, Manal, Arabi, Mariam, Refaat, Marwan M., DePalma, Steven R., Seidman, J. G., Seidman, Christine E., Bitar, Fadi F., Nemer, Georges M.

Journal:

Scientific Reports

Year:

2015

Language:

english

File:

PDF, 647 KB

english, 2015

5

Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy

Fahed, Akl C., Khalaf, Ruby, Salloum, Rony, Andary, Rabih R., Safa, Raya, El-Rassy, Inaam, Moubarak, Elie, Azar, Sami T., Bitar, Fadi F., Nemer, Georges

Journal:

Molecular Genetics & Genomic Medicine

Year:

2016

Language:

english

File:

PDF, 658 KB

english, 2016

6

Heart Failure in Congenital Heart Disease

Fahed, Akl C., Roberts, Amy E., Mital, Seema, Lakdawala, Neal K.

Journal:

Heart Failure Clinics

Year:

2014

Language:

english

File:

PDF, 586 KB

english, 2014

7

The Lebanese allele at theLDLRin normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia

Fahed, Akl C., Bitar, Fadi F., Khalaf, Ruby I., Moubarak, Elie M., Azar, Sami T., Nemer, Georges M.

Journal:

Endocrine (Springer)

Year:

2012

Language:

english

File:

PDF, 230 KB

english, 2012

8

ATHEROSCLEROTIC CARDIOVASCULAR DISEASE RISK IN ADULTS WITH CONGENITAL HEART DISEASE

Flannery, Laura, Fahed, Akl, Barinsky, Gregory, Youniss, Mohamed, Yeh, Doreen Defaria, Bhatt, Ami

Journal:

Journal of the American College of Cardiology

Year:

2016

Language:

english

File:

PDF, 400 KB

english, 2016

9

Yellow plaques on the hands of a 10-year-old girl

Saliba, Elie C., Fahed, Akl C.

Journal:

Journal of the American Academy of Dermatology

Year:

2017

Language:

english

File:

PDF, 297 KB

english, 2017

10

Frequency of Guideline-Based Statin Therapy in Adults with Congenital Heart Disease

Flannery, Laura D., Fahed, Akl C., Yeh, Doreen DeFaria, Youniss, Mohamed A., Barinsky, Gregory L., Stefanescu Schmidt, Ada C., Benavidez, Oscar J., Meigs, James B., Bhatt, Ami B.

Journal:

The American Journal of Cardiology

Year:

2017

Language:

english

File:

PDF, 867 KB

english, 2017

11

Pregnancy in a Woman with Homozygous Familial Hypercholesterolemia Not on Low-Density Lipoprotein Apheresis

Fahed, Akl, Nassar, Anwar

Journal:

American Journal of Perinatology Reports

Year:

2012

Language:

english

File:

PDF, 63 KB

english, 2012

12

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

Kamar, Amina, Fahed, Akl C., Shibbani, Kamel, El-Hachem, Nehme, Bou-Slaiman, Salim, Arabi, Mariam, Kurban, Mazen, Seidman, Jonathan G., Seidman, Christine E., Haidar, Rachid, Baydoun, Elias, Nemer, Ge

Journal:

Frontiers in Genetics

Year:

2017

Language:

english

File:

PDF, 1.73 MB

english, 2017

13

GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient

Kassab, Kameel, Hariri, Hadla, Gharibeh, Lara, Fahed, Akl C., Zein, Manal, El-Rassy, Inaam, Nemer, Mona, El-Rassi, Issam, Bitar, Fadi, Nemer, Georges

Journal:

Molecular Genetics & Genomic Medicine

Year:

2016

Language:

english

File:

PDF, 763 KB

english, 2016

14

Physiology as a Lingua Franca for Clinical Machine Learning

Sarma, Gopal P., Reinertsen, Erik, Aguirre, Aaron, Anderson, Chris, Batra, Puneet, Choi, Seung-Hoan, Di Achille, Paolo, Diamant, Nathaniel, Ellinor, Patrick, Emdin, Connor, Fahed, Akl C., Friedman, Sa

Journal:

Year:

2020

File:

PDF, 245 KB

2020

15

Homozygous familial hypercholesterolemia in Lebanon: A genotype/phenotype correlation

Akl C. Fahed, Raya M. Safa, Fadi F. Haddad, Fadi F. Bitar, Rabih R. Andary, Mariam T. Arabi, Sami T. Azar, Georges Nemer

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 435 KB

english, 2011

16

Students’ Perceptions of Peer-Organized Extra-Curricular Research Course during Medical School: A Qualitative Study

Nazha, Bassel, Salloum, Rony H., Fahed, Akl C., Nabulsi, Mona, Sapino, Anna

Journal:

Year:

2015

Language:

english

File:

PDF, 124 KB

english, 2015

17

PEDIATRIC CARDIOMYOPATHY MUTATIONS IN A HIGHLY CONSANGUINEOUS POPULATION

Fahed, Akl C., Candan, Şükrü, Haghighi, Alireza, DePalma, Steven, McDonough, Barbara, Erer, Betül, Ekmekçi, Ahmet, Bornaun, Helen, Öztarhan, Kazum, Aydin, Hatip, Seidman, Jonathan, Seidman, Christine

Journal:

Journal of the American College of Cardiology

Year:

2016

Language:

english

File:

PDF, 370 KB

english, 2016

18

Degenerated Hair Follicle Cells and Partial Loss of Sebaceous and Eccrine Glands in a Familial Case of Axenfeld-Rieger Syndrome: An Emerging Role for the FOXC1/NFATC1 Genetic Axis

Hariri, Hadla, Kurban, Mazen, Al-Haddad, Christiane, Fahed, Akl C., Poladian, Sarin, Kahlil, Athar, Abbas, Oussama, Arabi, Mariam, Bitar, Fadi, Nemer, Georges

Journal:

Journal of Dermatological Science

Year:

2018

File:

PDF, 466 KB

2018

19

Familial Hypercholesterolemia: The Lipids or the Genes?

Akl C Fahed, Georges M Nemer

Journal:

Nutrition & Metabolism

Year:

2011

Language:

english

File:

PDF, 887 KB

english, 2011

20

THE R21C MUTATION IN TROPONIN I HAS A FOUNDER EFFECT IN SOUTH LEBANON AND CAUSES MALIGNANT HYPERTROPHIC CARDIOMYOPATHY

Fahed, Akl, Nemer, Georges, Bitar, Fadi F., Arnaout, Samir, Abchee, Antoine B., Ware, James, Batrawi, Manal, DePalma, Steven R., McDonough, Barbara, Arabi, Mariam T., Seidman, Jonathan, Seidman, Chris

Journal:

Journal of the American College of Cardiology

Year:

2015

Language:

english

File:

PDF, 243 KB

english, 2015

21

Connecting the Lines between Hypogonadism and Atherosclerosis

Fahed, Akl C., Gholmieh, Joanna M., Azar, Sami T.

Journal:

International Journal of Endocrinology

Year:

2012

Language:

english

File:

PDF, 552 KB

english, 2012

22

The Muscle-Bound Heart

Refaat, Marwan M., Fahed, Akl C., Hassanieh, Sylvana, Hotait, Mostafa, Arabi, Mariam, Skouri, Hadi, Seidman, Jonathan G., Seidman, Christine E., Bitar, Fadi F., Nemer, Georges

Journal:

Cardiac Electrophysiology Clinics

Year:

2016

Language:

english

File:

PDF, 743 KB

english, 2016

23

Founder Mutation in N-terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy

Fahed, Akl C., Nemer, Georges, Bitar, Fadi F., Arnaout, Samir, Abchee, Antoine B., Batrawi, Manal, Khalil, Athar, Abou-Hassan, Oussama, DePalma, Steven R., McDonough, Barbara, Arabi, Mariam T., Ware,

Journal:

Circulation: Genomic and Precision Medicine

Year:

2020

File:

PDF, 496 KB

2020

24

Subclinical Burden of Coronary Artery Calcium in Patients with Coarctation of the Aorta

Krishnamurthy, Yamini, Stefanescu Schmidt, Ada C., Bittner, Daniel O., Scholtz, Jan-Erik, Bui, Amy, Reddy, Rajesh, Youniss, Mohamed A., Donohoe, Kendall, Flannery, Laura D., Fahed, Akl C., Ghoshhajra,

Journal:

The American Journal of Cardiology

Year:

2018

Language:

english

File:

PDF, 574 KB

english, 2018

25

A novel nonsense mutation inNPHS1: is aortic stenosis associated with congenital nephropathy?

GHARIBEH, LARA, EL-RASSY, INAAM, SOUBRA, AYMAN, SAFA, RAYA, FAHED, AKL, TANOS, RACHEL, ARABI, MARIAM, KAMBRIS, ZAKARIA, BITAR, FADI, NEMER, GEORGES

Journal:

Journal of Genetics

Year:

2015

Language:

english

File:

PDF, 410 KB

english, 2015

26

Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia

Fahed, Akl C., Shibbani, Kamel, Andary, Rabih R., Arabi, Mariam T., Habib, Robert H., Nguyen, Denis D., Haddad, Fady F., Moubarak, Elie, Nemer, Georges, Azar, Sami T., Bitar, Fadi F.

Journal:

Year:

2017

Language:

english

File:

PDF, 1.41 MB

english, 2017

27

Diet, Genetics, and Disease: A Focus on the Middle East and North Africa Region

Fahed, Akl C., El-Hage-Sleiman, Abdul-Karim M., Farhat, Theresa I., Nemer, Georges M.

Journal:

Journal of Nutrition and Metabolism

Year:

2012

Language:

english

File:

PDF, 980 KB

english, 2012

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