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The cooperative international neuromuscular research group Duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures
The cooperative international neuromuscular research group Duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures
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The cooperative international neuromuscular research group Duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures

Henricson, Erik K. ; Abresch, R. Ted ; Cnaan, Avital ; Hu, Fengming ; Duong, Tina ; Arrieta, Adrienne ; Han, Jay ; Escolar, Diana M. ; Florence, Julaine M. ; Clemens, Paula R. ; Hoffman, Eric P. ; McDonald, Craig M.

Muscle & nerve, 2013-07, Vol.48 (1), p.55-67 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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2
N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children
N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children
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N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children

Wright, Sukhvir ; Hacohen, Yael ; Jacobson, Leslie ; Agrawal, Shakti ; Gupta, Rajat ; Philip, Sunny ; Smith, Martin ; Lim, Ming ; Wassmer, Evangeline ; Vincent, Angela

Archives of disease in childhood, 2015-06, Vol.100 (6), p.521-526 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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3
Turner syndrome in diverse populations
Turner syndrome in diverse populations
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Turner syndrome in diverse populations

Kruszka, Paul ; Addissie, Yonit A. ; Tekendo‐Ngongang, Cedrik ; Jones, Kelly L. ; Savage, Sarah K. ; Gupta, Neerja ; Sirisena, Nirmala D. ; Dissanayake, Vajira H. W. ; Paththinige, C. Sampath ; Aravena, Teresa ; Nampoothiri, Sheela ; Yesodharan, Dhanya ; Girisha, Katta M. ; Patil, Siddaramappa Jagdish ; Jamuar, Saumya Shekhar ; Goh, Jasmine Chew‐Yin ; Utari, Agustini ; Sihombing, Nydia ; Mishra, Rupesh ; Chitrakar, Neer Shoba ; Iriele, Brenda C. ; Lulseged, Ezana ; Megarbane, Andre ; Uwineza, Annette ; Oyenusi, Elizabeth Eberechi ; Olopade, Oluwarotimi Bolaji ; Fasanmade, Olufemi Adetola ; Duenas‐Roque, Milagros M. ; Thong, Meow‐Keong ; Tung, Joanna Y. L. ; Mok, Gary T. K. ; Fleischer, Nicole ; Rwegerera, Godfrey M. ; Herreros, María Beatriz ; Watts, Johnathan ; Fieggen, Karen ; Huckstadt, Victoria ; Moresco, Angélica ; Obregon, María Gabriela ; Hussen, Dalia Farouk ; Ashaat, Neveen A. ; Ashaat, Engy A. ; Chung, Brian H. Y. ; Badoe, Eben ; Faradz, Sultana M. H. ; El Ruby, Mona O. ; Shotelersuk, Vorasuk ; Wonkam, Ambroise ; Ekure, Ekanem Nsikak ; Phadke, Shubha R. ; Richieri‐Costa, Antonio ; Muenke, Maximilian

American journal of medical genetics. Part A, 2020-02, Vol.182 (2), p.303-313 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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