E. Kochova

Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature

M. Kocova, E. Kochova, E. Sukarova-Angelovska, 2015, BMC Endocrine Disorders.

Investigating the clinico-anatomical dissociation in the behavioral variant of Alzheimer disease

B. Miller, P. Scheltens, F. Barkhof, 2019, Alzheimer's research & therapy.

Synapsin-antibodies in psychiatric and neurological disorders: Prevalence and clinical findings

R. Mertens, F. Benfenati, F. Paul, 2017, Brain, Behavior, and Immunity.

X-Linked Adrenoleukodystrophy: Diagnostic and Therapeutic Approach

E. Kochova, 2017 .

Epitope specificity of anti-synapsin autoantibodies: Differential targeting of synapsin I domains

R. Mertens, F. Benfenati, M. Höltje, 2018, PloS one.

Rare case of Killian-Pallister syndrome associated with idiopathic short stature detected with fluorescent in situ hybridization on buccal smear

M. Kocova, E. Kochova, E. Sukarova-Angelovska, 2016, Molecular Cytogenetics.

Autoimmune thyroiditis and thyroid cancer in a child with lymphocytic infundibuloneurohypophysitis

M. Kocova, E. Kochova, Pop Gjorcheva, 2016 .

Diagnostic approach in children with unusual symptoms of acquired hypothyroidism. When to look for pituitary hyperplasia?

M. Kocova, E. Kochova, R. Kacarska, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Rare case of Killian-Pallister syndrome associated with idiopathic short stature detected with fluorescent in situ hybridization on buccal smear

M. Kocova, E. Kochova, E. Sukarova-Angelovska, 2016, Molecular Cytogenetics.