Search Results - ( fautorsss OR (( (factossrss OR acto) OR ( case OR (autor OR actos) )) OR factories ))*

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    Spondylothoracic dysostosis, Jarcho Levin syndrome: case report by Medina de la Cruz, Antonia Yesenia, Rodríguez Balderrama, Isaías, Burciaga Flores, Carlos Horacio, Martínez de Villarreal, Laura Elia, Ibarra Ramírez, Marisol, O Cavazos, Manuel Enrique de la

    Published 2016
    “…It is inherited in an autosomal recessive manner and the only related gene is MESP2. Clinical case: Newborn male, who during the first hour of life develops perioral cyanosis, thoracoabdominal dissociation and polipnea, requiring endotracheal intubation and mechanical ventilation for respiratory impairment, finding thoracoabdominal costovertebral abnormalities with an x-ray, and a conditioning restrictive pattern like a crab. …”
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  3. 123

    Composición factorial de la escala de ansiedad ante el envejecimiento de lasher y faulkender en estudiantes universitarios mexicanos by Ornelas, Martha, Gastélum Cuadras, Gabriel, López Walle, Jeanette M., Rodríguez Villalobos, Judith Margarita

    Published 2016
    “…Los análisis, muestran que una estructura tetra factorial es adecuada ya que a través de criterios estadísticos y sustantivos, ha mostrado adecuados indicadores de fiabilidad y validez. …”
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    Réquiem por el poeta romano Ovidio, autor de las metamorfosis by Puente Sánchez, Enrique

    Published 2025
    “…Uno de ellos es Publio Virgilio Marón, autor de La Eneida, epopeya en doce libros que el poeta no alcanzó a pulir como él quería: la muerte se lo impidió. …”
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  7. 127

    Congenital fiber-type disproportion myopathy: a case study by Haro Hernández, B. J. de, Macouzet Sánchez, Carlos, Rodríguez Balderrama, Isaías, O Cavazos, Manuel Enrique de la

    Published 2015
    “…The following describes the case of a patient who was born in the ‘‘Dr. José Eleuterio González’’ University Hospital in Monterrey, N.L, who presented clinical and muscle biopsy compatible with this myopathy.…”
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  8. 128

    Case report: Diagnostic reconceptualization in the DSM-V on somatoform disorders by Ibarra Patrón, Diana, Medina Vidales, Guillermo, Garza Guerrero, C.

    Published 2015
    “…These patients often turn to different general practitioners and/or non-psychiatric specialists for long periods of time and represent a diagnostic and therapeutic challenge, as the possible organic component makes it complex and difficult to manage. The reported case is a 24-year-old male patient with a diagnosis of Somatic Symptoms Disorder and multiple psychiatric comorbidities. …”
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  9. 129

    Self-inflicted wound with a nail in the heart: case report by Reyna Sepúlveda, Francisco J., Cueto Ramos, Rubén Gerardo, Vásquez Fernández, Francisco, Hernández Guedea, Marco Antonio, Guevara Charles, Asdrúbal, Muñoz Maldonado, Gerardo Enrique

    Published 2016
    “…It is estimated that more than 90% of mortality happens before the patient reaches the hospital and only 15---50% of those will receive appropriate medical treatment. Case report: A 42-year-old hemodynamically stable male is brought to the ED with a protruding nail in his thorax. …”
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  10. 130

    Laparoscopic diaphragmatic plication for paralysis posterior to trauma. Case report by Reyna Sepúlveda, Francisco J., Vásquez Fernández, Francisco, Rodríguez Briseño, José Ángel, Moreno Cantú, Carlos Alberto, Muñoz Maldonado, Gerardo Enrique

    Published 2016
    “…Laparoscopic diaphragmatic plicature is a safe procedure associated with a minimal hospital stay, and more cases need to be reported. This is the procedure of choice in our institution.…”
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    An unusually severe Case of dermatosis neglecta: a diagnostic challenge by Pérez Rodríguez, Irma Margarita, Muñoz Garza, Fania Zamantta, Ocampo Candiani, Jorge

    Published 2014
    “…Dermatosis neglecta is a condition secondary to lack of cleanliness, characterized by the formation of hyperkeratotic plaques located in a particular region of the body, usually due to a disability, and it is considered a diagnostic challenge because it can mimic other entities. We present the case of an 18-year-old woman with a 2-month history of progressive brown verrucous plaque in her face. …”
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    A Fatal Case of Generalized Lysosomal Storage Disease in an Infant. by Ponce Camacho, Marco Antonio, Melo de la Garza, Américo, Barboza Quintana, Álvaro, Barboza Quintana, Oralia, Ancer Rodríguez, Jesús, Ramírez Bon, Enrique, Garza Alatorre, Arturo Gerardo, Rodríguez Gutiérrez, Nora Alicia

    Published 2010
    “…Depending on the severity of the enzymatic defect, gangliosidoses show different rates of clinical progression and organ involvement; poor residual enzyme activity is seen in more aggressive forms (infantile and juvenile subtypes) leading to early death whereas cases with better residual enzyme activity have a late onset in adult life and a milder clinical course. …”
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