Hypoparathyroidism in an Egyptian child with Hutchinson-Gilford progeria syndrome: a case report.

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The epidemiology of premature aging and associated comorbidities A systematic approach to the magnetic resonance imaging-based differential diagnosis of congenital Müllerian duct anomalies and their mimics.Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort.

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Hypoparathyroidism in an Egyptian child with Hutchinson-Gilford progeria syndrome: a case report.

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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P1476

Hypoparathyroidism in an Egypt ...... geria syndrome: a case report.

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P2093

Hekma Saad Fargalley

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Kotb Abbass Metwalley Kalil

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P2860

Phenotype and course of Hutchinson-Gilford progeria syndrome

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome

Hutchinson-Guilford progeria syndrome

Congenital Absence of Hair and Mammary Glands with Atrophic Condition of the Skin and its Appendages, in a Boy whose Mother had been almost wholly Bald from Alopecia Areata from the age of Six.

Progeria: a cell culture study on aging

LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome.

Progeria.

The Hutchinson-Gilford progeria syndrome. Report of 4 cases and review of the literature.

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome.

Case report: extensive brain calcification in hypoparathyroidism.

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scholarly article

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10.1186/1752-1947-6-17

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English

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2012-01-17T00:00:00Z

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221753716

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Hypoparathyroidism in an Egyptian child with Hutchinson-Gilford progeria syndrome: a case report.

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P2860

P2860

Hypoparathyroidism in an Egyptian child with Hutchinson-Gilford progeria syndrome: a case report.

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P5875

P698

P932