Spinal muscular atrophy: foetal-like histopathological pattern in Werdnig-Hoffmann disease.

Por Hausmanowa-Petrusewicz, I, Fidzianska, A
Publicado em 1974

Looking for disease being a model of human aging

Por Hausmanowa-Petrusewicz, I, Madej-Pilarczyk, A
Publicado em 2007

Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.

Por Hausmanowa-Petrusewicz, I, Zaremba, J, Borkowska, J
Publicado em 1985

O-5. A wide spectrum of phenotypes in recessive forms of Charcot-Marie-Tooth disorders with known and unknown etiology in Poland

Por Kochański, A, Kabzińska, D, Hausmanowa-Petrusewicz, I
Publicado em 2009

Chronic proximal spinal muscular atrophy of childhood and adolescence: sex influence.

Por Hausmanowa-Petrusewicz, I, Zaremba, J, Borkowska, J, Szirkowiec, W
Publicado em 1984

Age-related change in duration of afterhyperpolarization of human motoneurones

Por Piotrkiewicz, M, Kudina, L, Mierzejewska, J, Jakubiec, M, Hausmanowa-Petrusewicz, I
Publicado em 2007

Circulating autoantibodies to troponin I in Emery-Dreifuss muscular dystrophy

Por Niebroj-Dobosz, I, Marchel, M, Madej, A, Sokolowska, B, Hausmanowa-Petrusewicz, I
Publicado em 2008

Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene

Por Kabzińska, D, Saifi, GM, Drac, H, Rowińska-Marcińska, K, Hausmanowa-Petrusewicz, I, Kochański, A, Lupski, JR
Publicado em 2007

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

Por Yates, J R, Affara, N A, Jamieson, D M, Ferguson-Smith, M A, Hausmanowa-Petrusewicz, I, Zaremba, J, Borkowska, J, Johnston, A W, Kelly, K
Publicado em 1986

Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.

Por Brzustowicz, L M, Wang, C H, Matseoane, D, Kleyn, P W, Vitale, E, Das, K, Penchaszadeh, G K, Munsat, T L, Hausmanowa-Petrusewicz, I, Gilliam, T C
Publicado em 1995

Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

Por Yates, J R, Warner, J P, Smith, J A, Deymeer, F, Azulay, J P, Hausmanowa-Petrusewicz, I, Zaremba, J, Borkowska, J, Affara, N A, Ferguson-Smith, M A
Publicado em 1993

Molecular genetic and genetic correlations in sodium channelopathies: Lack of founder effect and evidence for a second gene

Por Wang, J., Zhou, J., Todorovic, S. M., Feero, W. G., Barany, F., Conwit, R., Hausmanowa-Petrusewicz, I., Fidzianska, A., Arahata, K., Wessel, H. B., Sillen, A., Marks, H. G., Hartlage, P., Galloway, G., Ricker, K., Lehmann-Horn, F., Hayakawa, H., Hoffman, E. P.
Publicado em 1993

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

Por Zimoń, M., Baets, J., Fabrizi, G.M., Jaakkola, E., Kabzińska, D., Pilch, J., Schindler, A.B., Cornblath, D.R., Fischbeck, K.H., Auer-Grumbach, M., Guelly, C., Huber, N., De Vriendt, E., Timmerman, V., Suter, U., Hausmanowa-Petrusewicz, I., Niemann, A., Kochański, A., De Jonghe, P., Jordanova, A.
Publicado em 2011