Klára Roženková

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.

P. Njølstad, K. Hussain, Z. Šumník, 2015, The Journal of clinical endocrinology and metabolism.

Severe Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Paternal Uniparental Disomy of 11p15.5 Managed with Sirolimus Therapy

K. Hussain, M. Güemes, K. Morgan, 2016, Hormone Research in Paediatrics.

Ad Dress for Cor Res Pon Den Ce

K. Hussain, M. Güemes, P. Shah, 2022 .

Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families

P. Kučerová, S. Pruhova, J. Lebl, 2020, Hormone Research in Paediatrics.

[Congenital hyperinsulinism: Loss of B-cell self-control].

S. Pruhova, J. Lebl, Klára Roženková, 2016, Vnitrni lekarstvi.

Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial.

E. Bertini, F. Aarsen, L. de Meirleir, 2019, The lancet. Diabetes & endocrinology.

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study.

E. Bertini, N. Brunetti‐Pierri, M. Polak, 2020, The lancet. Diabetes & endocrinology.

Quality of Life and Treatment Satisfaction in Participants with Maturity-Onset Diabetes of the Young: A Comparison to Other Major Forms of Diabetes.

O. Cinek, Z. Šumník, S. Pruhova, 2020, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia

K. Hussain, M. Güemes, P. Shah, 2015, Journal of clinical research in pediatric endocrinology.