M. Bernardini

Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS).

R. Reithmeier, J. Jaeken, H. Schachter, 1995, European journal of biochemistry.

Bullous‐vesicular variant of mycosis fungoides presenting as erythema annulare centrifugum: a case report

A. Offidani, A. Campanati, M. Giangiacomi, 2009, Journal of the European Academy of Dermatology and Venereology : JEADV.

ABCB1 c.-6-180T>G polymorphism and clinical risk factors in a multi-breed cohort of dogs with refractory idiopathic epilepsy.

M. Turba, A. Cauduro, M. Menchetti, 2019, Veterinary journal.