Results 121 to 126 of about 2,064 (126)

Diagnostic value of multiple café‐au‐lait macules for neurofibromatosis 1 in Chinese children

Journal of Dermatology, 2016
Ru-en Yao, Yongguo Yu, Yiping Shen
exaly  

A severe form of Noonan syndrome and autosomal dominant café‐au‐lait spots – evidence for different genetic origins

Acta Paediatrica, International Journal of Paediatrics, 2009
Ann-Charlotte Thuresson
exaly  

Association of Piebaldism, Multiple Café‐au‐lait Macules, and Intertriginous Freckling: Clinical Evidence of a Common Pathway between KIT and Sprouty‐Related, Ena/Vasodilator‐Stimulated Phosphoprotein Homology‐1 Domain Containing Protein 1 (SPRED1)

Pediatric Dermatology, 2013
Yvonne E Chiu
exaly  

Choroidal abnormalities in café‐au‐lait syndromes: a new differential diagnostic tool?

Clinical Genetics, 2017
exaly  

Les résidus d’antibiotiques dans le lait cru de vache : état des lieux dans la région de l’Ouest Algérien

Journal De La Faculté De Médecine D'Oran
exaly  

The mechanism of epidermal hyperpigmentation in cafe-au-lait macules of neurofibromatosis type 1 (von Recklinghausen's disease) may be associated with dermal fibroblast-derived stem cell factor and hepatocyte growth factor

British Journal of Dermatology, 2003
exaly