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U Yamamoto

Showing results (1-10 of 10) with videos related to

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Sao Paulo Medical Journal = Revista Paulista De Medicina|January 7, 1999
Variations in white blood count, thromboxane B2 levels and hematocrit in chronic venous hypertensionP C Guimarães, P Puech-Leão, B M Netto, et al.
Zootaxa|July 6, 2026
<b>Morphological revision of the species of <i>Homoeomma</i> Ausserer, 1871 (Araneae: Theraphosidae) from Brazil, Argentina and Uruguay</b>Arthur Galleti-Lima, Flávio U Yamamoto, Sylvia M Lucas, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 24, 2004
Protein and DNA analysis for the prenatal diagnosis of alpha2-laminin-deficient congenital muscular dystrophyLydia U Yamamoto, Thomas R Gollop, Nadyr F Naccache, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 23, 2008
Muscle protein alterations in LGMD2I patients with different mutations in the Fukutin-related protein geneLydia U Yamamoto, Fernando J Velloso, Bruno L Lima, et al.
Muscle & Nerve|January 17, 2012
Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotypeJuliana Gurgel-Giannetti, Adriano S Senkevics, Dinorah Zilbersztajn-Gotlieb, et al.
Journal of Molecular Neuroscience : MN|January 19, 2008
Animal models for genetic neuromuscular diseasesMariz Vainzof, Danielle Ayub-Guerrieri, Paula C G Onofre, et al.
BMC Research Notes|August 3, 2014
Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case reportThais Cuperman, Stephanie A Fernandes, Naila C V Lourenço, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|June 8, 2001
The patient-physician interactions as seen by undergraduate medical studentsL Y Kiyohara, L K Kayano, M L Kobayashi, et al.
BMC Clinical Pathology|October 10, 2014
Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image patternAna Cotta, Julia Filardi Paim, Antonio Lopes da-Cunha-Junior, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centersMariz Vainzof, Pascale Richard, Ralf Herrmann, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Sao Paulo Medical Journal = Revista Paulista De Medicina|January 7, 1999
Variations in white blood count, thromboxane B2 levels and hematocrit in chronic venous hypertensionP C Guimarães, P Puech-Leão, B M Netto, et al.
Zootaxa|July 6, 2026
<b>Morphological revision of the species of <i>Homoeomma</i> Ausserer, 1871 (Araneae: Theraphosidae) from Brazil, Argentina and Uruguay</b>Arthur Galleti-Lima, Flávio U Yamamoto, Sylvia M Lucas, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 24, 2004
Protein and DNA analysis for the prenatal diagnosis of alpha2-laminin-deficient congenital muscular dystrophyLydia U Yamamoto, Thomas R Gollop, Nadyr F Naccache, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 23, 2008
Muscle protein alterations in LGMD2I patients with different mutations in the Fukutin-related protein geneLydia U Yamamoto, Fernando J Velloso, Bruno L Lima, et al.
Muscle & Nerve|January 17, 2012
Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotypeJuliana Gurgel-Giannetti, Adriano S Senkevics, Dinorah Zilbersztajn-Gotlieb, et al.
Journal of Molecular Neuroscience : MN|January 19, 2008
Animal models for genetic neuromuscular diseasesMariz Vainzof, Danielle Ayub-Guerrieri, Paula C G Onofre, et al.
BMC Research Notes|August 3, 2014
Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case reportThais Cuperman, Stephanie A Fernandes, Naila C V Lourenço, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|June 8, 2001
The patient-physician interactions as seen by undergraduate medical studentsL Y Kiyohara, L K Kayano, M L Kobayashi, et al.
BMC Clinical Pathology|October 10, 2014
Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image patternAna Cotta, Julia Filardi Paim, Antonio Lopes da-Cunha-Junior, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centersMariz Vainzof, Pascale Richard, Ralf Herrmann, et al.
Pageof 1