Lídia Balogh

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Martina Živná, Kendrah Kidd, Mohamad Zaidan et al. · Kidney International · 2020 · 39 citations · Full text

Glomerular Disease, Glomerulonephritis, Urology +11

Severe Hyperinsulinemic Hypoglycemia in a Neonate: Response to Sirolimus Therapy

Ünőke Méder, Géza Bokodi, Lídia Balogh et al. · PEDIATRICS · 2015 · 24 citations · Full text

Metabolic Syndrome, Severe Hypoglycemia, Rapamycin Inhibitor +14

Relation between biomarkers and clinical severity in patients with Smith–Lemli–Opitz syndrome

Anna V. Oláh, Gabriella P. Szabó, József Varga et al. · European Journal of Pediatrics · 2013 · 22 citations · Full text

Clinical Disorders, Smith–lemli–opitz Syndrome, Diagnosis +2

A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia

M. Milt�nyi, Lídia Balogh, Katherine Schmidt et al. · European Journal of Pediatrics · 1984 · 21 citations

Thumb Hypoplasia, Ophthalmology, New Variant +2

Mutational Spectrum of Smith-Lemli-Opitz Syndrome Patients in Hungary

István Balogh, Katalin Koczok, György Szabó et al. · Molecular Syndromology · 2012 · 18 citations · Full text