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The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society|March 29, 2001
Management dilemmas in patients with hereditary renal adysplasiaE Morava, C Smith, M Pierce, et al.Journal of Inherited Metabolic Disease|January 7, 2004
Tall stature and progressive overweight in mitochondrial encephalopathyE Morava, F A Hol, A Janssen, et al.Acta Paediatrica Hungarica|January 1, 1983
Thyrotropin and prolactin response to thyrotropin-releasing hormone in healthy and asphyxiated full-term neonatesF Ruppert, M Adonyi, T Ertl, et al.JIMD Reports|February 23, 2013
Primary Carnitine (OCTN2) Deficiency Without Neonatal Carnitine DeficiencyL de Boer, L A J Kluijtmans, E MoravaActa Paediatrica Hungarica|January 1, 1986
Severe hypertension in a ten-year-old boy secondary to an aldosterone-producing tumour identified by adrenal sonographyT Decsi, G Soltész, F Harangi, et al.American Journal of Medical Genetics|April 5, 2000
Isodicentric Y chromosome in an Ullrich-Turner patient without virilizationE Morava, R Hermann, M Czakó, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomaliesE Morava, K E Jackson, F Tsien, et al.American Journal of Medical Genetics|August 3, 2001
Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomaliesM Riegel, E Morava, M Czakó, et al.American Journal of Medical Genetics|August 26, 1998
Report of a new patient with transposition of the great arteries with deletion of 22q11.2M Marble, E Morava, R Lopez, et al.Journal of Inherited Metabolic Disease|November 14, 2024
Assessing age of onset and clinical symptoms over time in patients with heterozygous pathogenic DHDDS variantsI J J Muffels, M Sadek, T Kozicz, et al.Pageof 9