[Reye's syndrome]

N Illum

Ugeskrift for Laeger

|June 30, 1986

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[Reye's syndrome]

Related Concept Videos

Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome.

Interferon-alfa treatment of facial infantile haemangiomas: with emphasis on the sight-threatening varieties. A clinical series.

Ulcerated haemangioma successfully treated with interferon alfa-2b and topical granulocyte-macrophage colony-stimulating factor.

Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.

A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)].

The role of Mycobacteria Other Than Tuberculosis (MOTT) in patients with cystic fibrosis.

[Mosaicism as a cause of Cowden syndrome].

[Thyrotoxic crisis with cardiogenic shock].

[Mindfulness-based cognitive therapy in the treatment of depression].

[Fitness].

[Risk of developing cataract related to fluoroscopy].

[Obturator hernia with small bowel ileus presenting as hip pain in an elderly woman].

Related Experiment Videos

[Reye's syndrome]

Related Concept Videos

Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome.

Interferon-alfa treatment of facial infantile haemangiomas: with emphasis on the sight-threatening varieties. A clinical series.

Ulcerated haemangioma successfully treated with interferon alfa-2b and topical granulocyte-macrophage colony-stimulating factor.

Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.

A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)].

The role of Mycobacteria Other Than Tuberculosis (MOTT) in patients with cystic fibrosis.

[Mosaicism as a cause of Cowden syndrome].

[Thyrotoxic crisis with cardiogenic shock].

[Mindfulness-based cognitive therapy in the treatment of depression].

[Fitness].

[Risk of developing cataract related to fluoroscopy].

[Obturator hernia with small bowel ileus presenting as hip pain in an elderly woman].

Related Experiment Videos

[Reye's syndrome]

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Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome.

Interferon-alfa treatment of facial infantile haemangiomas: with emphasis on the sight-threatening varieties. A clinical series.

Ulcerated haemangioma successfully treated with interferon alfa-2b and topical granulocyte-macrophage colony-stimulating factor.

Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.

A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)].

The role of Mycobacteria Other Than Tuberculosis (MOTT) in patients with cystic fibrosis.

[Mosaicism as a cause of Cowden syndrome].

[Thyrotoxic crisis with cardiogenic shock].

[Mindfulness-based cognitive therapy in the treatment of depression].

[Fitness].

[Risk of developing cataract related to fluoroscopy].

[Obturator hernia with small bowel ileus presenting as hip pain in an elderly woman].

Related Experiment Videos

[Reye's syndrome]

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Related Articles

Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome.

Interferon-alfa treatment of facial infantile haemangiomas: with emphasis on the sight-threatening varieties. A clinical series.

Ulcerated haemangioma successfully treated with interferon alfa-2b and topical granulocyte-macrophage colony-stimulating factor.

Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.

A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)].

The role of Mycobacteria Other Than Tuberculosis (MOTT) in patients with cystic fibrosis.

[Mosaicism as a cause of Cowden syndrome].

[Thyrotoxic crisis with cardiogenic shock].

[Mindfulness-based cognitive therapy in the treatment of depression].

[Fitness].

[Risk of developing cataract related to fluoroscopy].

[Obturator hernia with small bowel ileus presenting as hip pain in an elderly woman].