Literature DB >> 7712641

Tuberous sclerosis.

E S Roach1, M R Delgado.   

Abstract

Tuberous sclerosis complex is a disorder of cellular differentiation and proliferation that is inherited as an autosomal dominant trait with variable penetrance and a high spontaneous mutation rate. Lesions occur in the brain, skin, kidneys, heart, and other organs. Recent studies suggest genetic heterogeneity, with at least two gene loci on chromosomes 9, 16, and perhaps 11.

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Year:  1995        PMID: 7712641

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  3 in total

1.  Primitive neuroectodermal tumor in a child with tuberous sclerosis.

Authors:  B W Hindman; H K Gill; C W Zuppan
Journal:  Skeletal Radiol       Date:  1997-03       Impact factor: 2.199

Review 2.  Neurologic manifestations of tuberous sclerosis complex.

Authors:  William M McClintock
Journal:  Curr Neurol Neurosci Rep       Date:  2002-03       Impact factor: 5.081

3.  Tuberous sclerosis and polycystic kidney disease in a 3-month-old infant.

Authors:  Martin W Laass; Miriam Spiegel; Anna Jauch; Gabriele Hahn; Edgar Rupprecht; Christian Vogelberg; Oliver Bartsch; Angela Huebner
Journal:  Pediatr Nephrol       Date:  2004-03-09       Impact factor: 3.714

  3 in total

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