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Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment.

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Intravenous pamidronate treatment in children with moderate-to-severe osteogenesis imperfecta started under three years of age.

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Homocysteine and erythrocyte sedimentation rate correlate with cerebrovascular disease in fabry disease.

JIMD reports·2013

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Videos de Experimentos Relacionados

Clasificación de la osteogénesis imperfecta

Videos de Conceptos Relacionados

Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment.

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A common presentation of a rare genetic disorder clinically mimicking primary myopathy.

The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA.

Female external genitalia on fetal magnetic resonance imaging.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

[<sup>177</sup>Lu]Lu-edotreotide versus everolimus for gastroenteropancreatic neuroendocrine tumours (COMPETE): a phase 3, multicentre, randomised, open-label, superiority trial.

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Videos de Experimentos Relacionados

Clasificación de la osteogénesis imperfecta

Videos de Conceptos Relacionados

Artículos Relacionados

Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment.

Intravenous pamidronate treatment in children with moderate-to-severe osteogenesis imperfecta started under three years of age.

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A common presentation of a rare genetic disorder clinically mimicking primary myopathy.

The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA.

Female external genitalia on fetal magnetic resonance imaging.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

[<sup>177</sup>Lu]Lu-edotreotide versus everolimus for gastroenteropancreatic neuroendocrine tumours (COMPETE): a phase 3, multicentre, randomised, open-label, superiority trial.

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