Results 131 to 140 of about 888 (167)

Ichthyosis Uteri Associated with Endometrial Adenocarcinoma: A Case Report. [PDF]

open access: yesJ Clin Diagn Res, 2017
Bhardwaj N   +4 more
europepmc   +1 more source

Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndrome. [PDF]

open access: yesHum Genet
Soliman NA   +24 more
europepmc   +1 more source

Collodion baby with polydactyly. [PDF]

open access: yesIndian Dermatol Online J, 2015
Hassan I, Yaseen A, Ahmed K.
europepmc   +1 more source

The evolving spectrum of complex inherited neuropathies. [PDF]

open access: yesCurr Opin Neurol
Rossor AM, Haddad S, Reilly MM.
europepmc   +1 more source
Some of the next articles are maybe not open access.

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Harlequin icthyosis: report of one case

Archives of Gynecology and Obstetrics, 2009
Harlequin icthyosis is a rare extremely severe autosomal recessive dermatosis. The appearance of newborn can be shocking to parents and health care providers. Prenatal diagnosis is possible only with great suspicion and can often be missed. To our knowledge only 100 cases have been reported so far, we report one case of harlequin icthyosis.
Smiti Nanda
exaly   +3 more sources

Harlequin icthyosis with empyema thoracis

Indian Journal of Pediatrics, 1986
The rarest and most severe form of icthyosis and its association wth empyema thoracis is reported from Central India.
S, Thora   +4 more
exaly   +3 more sources

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