书信:卡尼缺乏症卡尼缺乏症

C Angelini

Lancet (London, England)

|September 20, 1975

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书信:卡尼缺乏症卡尼缺乏症

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Dysferlinopathy course and sportive activity: clues for possible treatment.

Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years.

Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiency.

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

Observation of the decay B- → D(s)((*)+) K- ℓ- ν(ℓ).

Search for production of invisible final states in single-photon decays of Υ(1S).

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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Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.

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书信:卡尼缺乏症卡尼缺乏症

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Dysferlinopathy course and sportive activity: clues for possible treatment.

Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years.

Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiency.

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

Observation of the decay B- → D(s)((*)+) K- ℓ- ν(ℓ).

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

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Dysferlinopathy course and sportive activity: clues for possible treatment.

Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years.

Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiency.

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

Observation of the decay B- → D(s)((*)+) K- ℓ- ν(ℓ).

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Dysferlinopathy course and sportive activity: clues for possible treatment.

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Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiency.

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

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书信:卡尼缺乏症卡尼缺乏症

书信:卡尼缺乏症卡尼缺乏症