Results 61 to 70 of about 6,571 (207)

Hypercalcemia in children: three cases report with unusual clinical presentations

open access: yesBrazilian Journal of Nephrology
Hypercalcemia is a rare condition in childhood; the most common causes are primary hyperparathyroidism, malignancy, prolonged immobilisation, thyrotoxicosis, thiazide diuretic, supplements containing calcium, milk-alkali syndrome, vitamin D intoxication,
Bruna Barros Garbim   +5 more
doaj   +1 more source

Estudio retrospectivo de pacientes con Gammapatía Monoclonal de Significado Incierto en el área de salud 6 de Valencia [PDF]

open access: yes, 2012
L'objectiu del present estudi va ser estudiar a la població afecta de GMSI en l'àrea de salut 6 de València, així com la incidència de la mateixa. Es tracta d'un estudi descriptiu transversal retrospectiu observacional dels pacients amb aquesta patologia
Monzó Castellano, Encarna   +4 more
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Disfunção miocárdica e alterações no trânsito de cálcio intracelular em ratos obesos

open access: yesArquivos Brasileiros de Cardiologia, 2011
FUNDAMENTO: Vários mecanismos têm sido propostos contribuir para a disfunção cardíaca em modelos de obesidade, tais como alterações nas proteínas do trânsito de cálcio (Ca+2) e nos receptores beta-adrenérgicos.
Ana Paula Lima-Leopoldo   +9 more
doaj  

Associação entre gamopatia monoclonal de significado indeterminado e hiperparatireoidismo primário no diagnóstico diferencial das hipercalcemias - Relato de caso

open access: yesBrazilian Journal of Nephrology, 2012
A gamopatia monoclonal de significado indeterminado (GMSI) é uma doença pré-maligna rara assintomática, definida por uma concentração de imunoglobulina monoclonal no soro menor que 3 g/dL e uma proporção de células plasmocitárias na medula óssea menor ...
Cristianne da Silva Alexandre   +5 more
doaj   +1 more source

Régulation de l'absorption intestinale du calcium chez le chamelon (Camelus dromedarius) [PDF]

open access: yes, 2003
L'hypercalcémie et l'hyperphosphatémie postprandiales, ainsi que l'absorption intestinale du calcium (Ca), ont été mesurées chez 12 chamelons. Les animaux ont été divisés en quatre groupes de trois individus.
Belhouari, Abderrahmane   +8 more
core   +2 more sources

Hypercalcemia and acute renal insufficiency following use of a veterinary supplement

open access: yesBrazilian Journal of Nephrology
A previously healthy 24 yo male presented with a two-month history of epigastric pain, nausea, vomiting, fatigue and malaise. He reported abuse of different substances, including an injectable veterinary vitamin compound, which contains high doses of ...
Marcelo Fernando Ronsoni   +7 more
doaj   +1 more source

HIPERPARATIROIDISMO PRIMARIO CLASICO SECUNDARIO A UN ADENOMA PARATIROIDEO

open access: yesBiociencias, 2018
Objetivo: Notificar un caso de hiperparatiroidismo primario sintomático secundario a un adenoma de paratiroideo. Caso: Femenina de 34 años con cuadro de 4 años de evolución con múltiples fracturas patológicas, pérdida de peso, astenia.
Jairo Rojano Rada
doaj   +1 more source

Use of Cinacalcet in the treatment of persistent hyperparathyroidism post-renal transplant. A single center experience in Argentina

open access: yesRevista de Nefrología, Diálisis y Trasplante, 2017
Introduction: Renal transplant (RTx) is associated with the decrease in serum parathyroidhormone (PTH) levels. The persistence of high PTH levels associated to hypercalcemia is suggestive of persistent hyperparathyroidism (pHPT).
Jorge Camacho   +4 more
doaj  

Hipercalcemia en el embarazo

open access: yesRevista Peruana de Ginecología y Obstetricia
Hyperparathyroidism during pregnancy is not a frequent diagnosis and is generally adiagnosis of exclusion. It may present with emetic episodes, alteration of the mentalsphere and of the state of consciousness, and abdominal pain. This causes difficultiesin its initial diagnosis and delay in starting treatment that leads to complicationssuch as ...
Luisa Fernanda Cano Bautista   +2 more
openaire   +1 more source

Síndrome de Williams-Beuren. Cuidados de enfermería [PDF]

open access: yes, 2016
El Síndrome de Williams es una enfermedad genética que compromete al tejido vascular, conectivo y al Sistema Nervioso Central. Presentando un perfil característico desde el punto de vista clínico, cognitivo, neurofisiológico y genético.
Arambillet González, María de Valdesalce
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