SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy
Pegoraro, E, Hoffman, E P, Piva, L, Gavassini, B F, Cagnin, S, Ermani, M, Bello, L, Soraru, G, Pacchioni, B, Bonifati, M D, Lanfranchi, G, Angelini, C, Kesari, A, Lee, I, Gordish-Dressman, H, Devaney, J M, McDonald, C M
Published in Neurology (18.01.2011)
Published in Neurology (18.01.2011)
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Association study of exome variants in the NF-κB and TGFβ pathways identifies CD40 as a modifier of Duchenne muscular dystrophy
Bello, L, Flanigan, K.M, Weiss, R.B, Spitali, P, Aartsma-Rus, A, Muntoni, F, Pegoraro, E, Gordish-Dressman, H, McDonald, C.M, Hoffman, E.P
Published in Neuromuscular disorders : NMD (01.10.2016)
Published in Neuromuscular disorders : NMD (01.10.2016)
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P4.12 AMPK and PPAR-delta agonists show beneficial effects in the mdx mouse model
Jahnke, V.E, Van Der Meulen, J.H, Johnston, H.K, Partridge, T, Hoffman, E.P, Nagaraju, K
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15
Martínez Murillo, F, Kobayashi, H, Pegoraro, E, Galluzzi, G, Creel, G, Mariani, C, Farina, E, Ricci, E, Alfonso, G, Pauli, R M, Hoffman, E P
Published in Neurology (13.07.1999)
Published in Neurology (13.07.1999)
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Molecular cloning, structure, and chromosomal localization of the human inducible nitric oxide synthase gene
CHARTRAIN, N. A, GELLER, D. A, KOTY, P. P, SITRIN, N. F, NUSSLER, A. K, HOFFMAN, E. P, BILLIAR, T. R, HUTCHINSON, N. I, MUDGETT, J. S
Published in The Journal of biological chemistry (04.03.1994)
Published in The Journal of biological chemistry (04.03.1994)
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Prevalence of Vitamin D Insufficiency in African-American Children with Forearm Fractures
Ryan, L.M, Brandoli, C, Freishtat, R.J, Chamberlain, J.M, Wright, J.L, Hoffman, E.P, Tosi, L
Published in Bone (New York, N.Y.) (01.06.2007)
Published in Bone (New York, N.Y.) (01.06.2007)
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Heart involvement in muscular dystrophies due to sarcoglycan gene mutations
Melacini, P., Fanin, M., Duggan, D.J., Freda, M.P., Berardinelli, A., Danieli, G.A., Barchitta, A., Hoffman, E.P., Volta, S. Dalla, Angelini, C.
Published in Muscle & nerve (01.04.1999)
Published in Muscle & nerve (01.04.1999)
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Cardiac transplantation in a Duchenne muscular dystrophy carrier
Melacini, P., Fanin, M., Angelini, A., Pegoraro, E., Livi, U., Danieli, G.A., Hoffman, E.P., Thiene, G., Dalla Volta, S., Angelini, C.
Published in Neuromuscular disorders : NMD (01.12.1998)
Published in Neuromuscular disorders : NMD (01.12.1998)
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P.27 - Association study of exome variants in the NF-κB and TGFβ pathways identifies CD40 as a modifier of Duchenne muscular dystrophy
Bello, L., Flanigan, K.M., Weiss, R.B., Spitali, P., Aartsma-Rus, A., Muntoni, F., Pegoraro, E., Gordish-Dressman, H., McDonald, C.M., Hoffman, E.P.
Published in Neuromuscular disorders : NMD (01.10.2016)
Published in Neuromuscular disorders : NMD (01.10.2016)
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Mosaic focal dermal hypoplasia caused by a novel somatic mutation in PORCN detected in affected skin
Sheu, J., Divito, S.J., Hoffman, E.P., Frank, N.Y., Merola, J.F.
Published in British journal of dermatology (1951) (01.08.2015)
Published in British journal of dermatology (1951) (01.08.2015)
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Decreased platelet expression of myosin regulatory light chain polypeptide (MYL9) and other genes with platelet dysfunction and CBFA2/RUNX1 mutation: insights from platelet expression profiling
SUN, L., GOROSPE, J. R., HOFFMAN, E. P., RAO, A. K.
Published in Journal of thrombosis and haemostasis (01.01.2007)
Published in Journal of thrombosis and haemostasis (01.01.2007)
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Adiposity attenuates muscle quality and the adaptive response to resistance exercise in non-obese, healthy adults
Peterson, M.D, Liu, D, Gordish-Dressman, H, Hubal, M.J, Pistilli, E, Angelopoulos, T.J, Clarkson, P.M, Moyna, N.M, Pescatello, L.S, Seip, R.L, Visich, P.S, Zoeller, R.F, Thompson, P.D, Devaney, J.M, Hoffman, E.P, Gordon, P.M
Published in International Journal of Obesity (01.08.2011)
Published in International Journal of Obesity (01.08.2011)
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Leptin and leptin receptor genetic variants associate with habitual physical activity and the arm body composition response to resistance training
Walsh, S., Haddad, C.J., Kostek, M.A., Angelopoulos, T.J., Clarkson, P.M., Gordon, P.M., Moyna, N.M., Visich, P.S., Zoeller, R.F., Seip, R.L., Bilbie, S., Thompson, P.D., Devaney, J., Gordish-Dressman, H., Hoffman, E.P., Price, Thomas B., Pescatello, L.S.
Published in Gene (15.11.2012)
Published in Gene (15.11.2012)
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Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder
Vanderver, A, Hathout, Y, Maletkovic, J, Gordon, E S, Mintz, M, Timmons, M, Hoffman, E P, Horzinski, L, Niel, F, Fogli, A, Boespflug-Tanguy, O, Schiffmann, R
Published in Neurology (03.06.2008)
Published in Neurology (03.06.2008)
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