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Refinado por: Nome da Publicação: American Journal of Medical Genetics (Neuropsychiatric Genetics) remover assunto: Biological And Medical Sciences remover
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Becker and limb-girdle muscular dystrophies: A psychiatric and intellectual level comparative study
Becker and limb-girdle muscular dystrophies: A psychiatric and intellectual level comparative study
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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?
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?
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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 mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder
Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder
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Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder

WASHIZUKA, Shinsuke ; KAKIUCHI, Chihiro ; MORI, Kanako ; KUNUGI, Hiroshi ; TAJIMA, Osamu ; AKIYAMA, Tsuyoshi ; NANKO, Shinichiro ; KATO, Tadafumi

American journal of medical genetics, 2003, Vol.120B (1), p.72-78

New York, NY: Wiley-Liss

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4
Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation
Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation
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Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation

Akiyama, Masaharu ; Kawame, Hiroshi ; Ohashi, Hirofumi ; Tohma, Takaya ; Ohta, Hidemi ; Shishikura, Akihiro ; Miyata, Ichiro ; Usui, Nobuo ; Eto, Yoshikatsu

American journal of medical genetics, 2001-03, Vol.99 (2), p.111-114

New York: John Wiley & Sons, Inc

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5
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
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The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females

Zatz, Mayana ; Marie, Suely K. ; Cerqueira, Antonia ; Vainzof, Mariz ; Pavanello, Rita C.M. ; Passos-Bueno, Maria Rita

American journal of medical genetics, 1998-05, Vol.77 (2), p.155-161

New York: John Wiley & Sons, Inc

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6
Association of polymorphism of serotonin 2A receptor gene with suicidal ideation in major depressive disorder
Association of polymorphism of serotonin 2A receptor gene with suicidal ideation in major depressive disorder
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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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7
Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls
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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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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8
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
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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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9
Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease
Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease
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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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10
An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease
An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease
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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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