Resultats de la cerca - Concetta Barone
- Mostrar 1 - 3 resultats de 3
-
1
Methionine synthase (MTR) 2756 (A → G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are... per Paolo Bosco, Rosa‐Maria Guéant‐Rodriguez, Guido Anello, Concetta Barone, Farès Namour, Filippo Caraci, Antonino Romano, Corrado Romano, Jean‐Louis Guéant
Publicat 2003Artigo -
2
Donor-Derived Strongyloides stercoralis Infection in Solid Organ Transplant Recipients in the United States, 2009–2013 per Francisca Abanyie, Elizabeth B. Gray, Kristin W. Delli Carpini, A. Yanofsky, Isabel McAuliffe, M Rana, Peter Chin‐Hong, Concetta Barone, Judy Davis, Susan P. Montgomery, Shirish Huprikar
Publicat 2015Artigo -
3
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant per David A. Koolen, Rolph Pfundt, Katrin Linda, Gea Beunders, Hermine E. Veenstra‐Knol, Jessie H. Conta, Ana María Fortuna, Gabriele Gillessen‐Kaesbach, Sarah Dugan, Sara Halbach, Omar Abdul‐Rahman, Heather M Winesett, Wendy K. Chung, Marguerite B. Dalton, Petia Dimova, Teresa Mattina, Katrina Prescott, Hui Z. Zhang, Howard M. Saal, Jayne Y. Hehir‐Kwa, Marjolein H. Willemsen, Charlotte W. Ockeloen, Marjolijn C.J. Jongmans, Nathalie Van der Aa, Pinella Failla, Concetta Barone, Emanuela Avola, Alice S. Brooks, Sarina G. Kant, Erica H. Gerkes, Helen V. Firth, Katrin Õunap, Lynne M. Bird, Diane Masser‐Frye, Jennifer Friedman, Modupe A Sokunbi, Abhijit Dixit, Miranda Splitt, Mary K. Kukolich, Julie McGaughran, Bradley P. Coe, Jesús Flórez, Nael Nadif Kasri, Han G. Brunner, Elizabeth M. Thompson, Jozef Gécz, Corrado Romano, Evan E. Eichler, Bert BA de Vries
Publicat 2015Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Internal medicine
Medicine
Allele
Amino acid
Asymptomatic
Biochemistry
Copy-number variation
Enzyme
Genome
Genotype
Haploinsufficiency
Helminths
Homocysteine
Hypotonia
Immunology
Immunosuppression
Intellectual disability
Loss of heterozygosity
MTRR
Methionine
Methionine synthase
Methylenetetrahydrofolate reductase
Microdeletion syndrome
Organ transplantation
Phenotype
Reductase
Strongyloides