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1
Becker and limb-girdle muscular dystrophies: A psychiatric and intellectual level comparative study
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Artigo
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Becker and limb-girdle muscular dystrophies: A psychiatric and intellectual level comparative study

Melo, Marcio ; Lauriano, Valèria ; Gentil, Valentim ; Eggers, Sabine ; Del Bianco, Sidionira Santos ; Gimenez, Paulo Rogério ; Akiyama, Jeanne ; Okabaiashi, Helena ; Frota-Pessoa, Oswaldo ; Passos-Bueno, Maria Rita ; Zatz, Mayana

American journal of medical genetics, 1995-02, Vol.60 (1), p.33-38 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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2
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?
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Artigo
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Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?

Eggers, Sabine ; Lauriano, Valèria ; Melo, Marcio ; Takata, Reinaldo Issao ; Akiyama, Jeanne ; Passos-Bueno, Maria Rita ; Gentil, Valentim ; Frota-Pessoa, Oswaldo ; Zatz, Mayana

American journal of medical genetics, 1995-02, Vol.60 (1), p.27-32 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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3
Association of polymorphism of serotonin 2A receptor gene with suicidal ideation in major depressive disorder
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Artigo
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Association of polymorphism of serotonin 2A receptor gene with suicidal ideation in major depressive disorder

Du, Lisheng ; Bakish, David ; Lapierre, Yvon D. ; Ravindran, Arun V. ; Hrdina, Pavel D.

American journal of medical genetics, 2000-02, Vol.96 (1), p.56-60 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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4
Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls
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Artigo
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Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls

Perry, Rodney T. ; Collins, Julianne S. ; Harrell, Lindy E. ; Acton, Ronald T. ; Go, Rodney C.P.

American journal of medical genetics, 2001-05, Vol.105 (4), p.332-342 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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5
Association of the C766T polymorphism of the low-density lipoprotein receptor-related protein gene with Alzheimer's disease
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Artigo
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Association of the C766T polymorphism of the low-density lipoprotein receptor-related protein gene with Alzheimer's disease

Kölsch, Heike ; Ptok, Ursula ; Mohamed, Iman ; Schmitz, Sandra ; Rao, Marie Luise ; Maier, Wolfgang ; Heun, Reinhard

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2003-08, Vol.121B (1), p.128-130 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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6
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
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Artigo
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Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia

Canki-Klain, Nina ; Milic, Astrid ; Kovac, Biserka ; Trlaja, Anuska ; Grgicevic, Damir ; Zurak, Niko ; Fardeau, Michel ; Leturcq, France ; Kaplan, Jean-Claude ; Urtizberea, J. Andoni ; Politano, Luisa ; Piluso, Giulio ; Feingold, Josue

American journal of medical genetics, 2004-03, Vol.125A (2), p.152-156 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease
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Artigo
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Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease

Alvarez, Victoria ; Mata, Ignacio F. ; González, Pelayo ; Lahoz, Carlos H. ; Martínez, Carmen ; Peña, Joaquín ; Guisasola, Luis M. ; Coto, Eliecer

American journal of medical genetics, 2002-07, Vol.114 (5), p.574-577 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease
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Artigo
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An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease

Rosenmann, Hanna ; Meiner, Zeev ; Kahana, Esther ; Aladjem, Zoja ; Friedman, Gideon ; Ben-Yehuda, Arie ; Grenader, Tal ; Wertman, Eli ; Abramsky, Oded

American journal of medical genetics, 2004-07, Vol.128B (1), p.123-125 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter
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Artigo
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Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter

Sarri, C. ; Gyftodimou, J. ; Avramopoulos, D. ; Grigoriadou, M. ; Pedersen, W. ; Pandelia, E. ; Pangalos, C. ; Abazis, D. ; Kitsos, G. ; Vassilopoulos, D. ; Brøndum-Nielsen, K. ; Petersen, M. B.

American journal of medical genetics, 1997-05, Vol.70 (1), p.87-94 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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10
Social adjustment in adult males affected with progressive muscular dystrophy
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Artigo
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Social adjustment in adult males affected with progressive muscular dystrophy

Eggers, Sabine ; Zatz, Mayana

American journal of medical genetics, 1998-02, Vol.81 (1), p.4-12 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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