疟疾中的免疫抑制.

Same author

Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiency.

Prenatal diagnosis·2001

Same author

Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.

Neuropediatrics·2001

Same author

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial.

Acta paediatrica (Oslo, Norway : 1992)·2001

Same author

Basal metabolic rate in children with a solid tumour.

European journal of clinical nutrition·2001

Same author

Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome.

Annals of human genetics·2001

Same author

Nuclear genes and oxidative phosphorylation disorders: a review.

European journal of pediatrics·2001

Same journal

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

Lancet (London, England)·2026

Same journal

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

Lancet (London, England)·2026

Same journal

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

Lancet (London, England)·2026

Same journal

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

Lancet (London, England)·2026

Same journal

Research priorities for characterising Bundibugyo virus.

Lancet (London, England)·2026

Same journal

Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.

Lancet (London, England)·2026

相关实验视频

疟疾中的免疫抑制.

相关概念视频

Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiency.

Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial.

Basal metabolic rate in children with a solid tumour.

Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome.

Nuclear genes and oxidative phosphorylation disorders: a review.

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.

Research priorities for characterising Bundibugyo virus.

Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.

相关实验视频

疟疾中的免疫抑制.

相关概念视频

相关文章

Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiency.

Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial.

Basal metabolic rate in children with a solid tumour.

Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome.

Nuclear genes and oxidative phosphorylation disorders: a review.

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.

Research priorities for characterising Bundibugyo virus.

Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.