Results 171 to 180 of about 24,840 (206)

Tuberous sclerosis complex

Current Opinion in Neurology, 2000
Tuberous sclerosis complex is an autosomal dominant disorder that causes significant complications in multiple organ systems. Both basic science and clinical research on tuberous sclerosis complex have flourished in recent years, improving our understanding of its molecular genetics and pathophysiology. Two tuberous sclerosis complex genes cause nearly
S P, Sparagana, E S, Roach
openaire   +2 more sources

Tuberous sclerosis complex

The Indian Journal of Pediatrics, 2004
16month-old-male child with history of hypo pigmented lesion with recurrent attacks of generalized episodes of tonic clonic convulsions since the age of 3 months with g lobal d e v e l o p m e n t a l de l ay (DQ a r o u n d 60) Well circumscribed hypo pigmented lesions 7 in no.
N M, Suryavanshi   +3 more
openaire   +2 more sources

Tuberous sclerosis complex

2018
Tuberous sclerosis complex (TSC) is an autosomal-dominant or sporadic multisystem disorder that results from mutations in either TSC1 or TSC2. The primary organs affected include the brain, skin, lung, kidney, and heart, all with variable frequency, penetrance, and severity.
Daphne M, Hasbani, Peter B, Crino
openaire   +2 more sources

The Tuberous Sclerosis Complex

Scottish Medical Journal, 1968
A typical case of tuberous sclerosis is described with the post-mortem findings. A suggestion is made to aid in the recognition of papilloedema.
openaire   +2 more sources

Tuberous Sclerosis Complex

Journal of Cutaneous Medicine and Surgery, 2023
Li-wen Zhang, Tao Chen
openaire   +3 more sources

Tuberous Sclerosis Complex

Urology, 2022
Luis Gabriel Vázquez-Lavista   +3 more
openaire   +2 more sources

Epstein–Barr virus and multiple sclerosis

Nature Reviews Microbiology, 2022
Samantha S Soldan, Paul M Lieberman
exaly  

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