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Publications by F Lorenzen

Late-Onset, Cryptic and Classical 21-Oh Deficiency: Allelic Variants

Pediatric Research

English

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Late Onset 21-Hydroxylase Deficiency Presenting as Pre-Pubertal Gynaecomastia

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Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

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High Diagnostic Yield and Novel Variants in Very Late-Onset Spasticity

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HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?

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HLA-E Allelic Variants

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Pathophysiologic Effects of CHCHD2 Variants Associated With Late-Onset Parkinson Disease

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Genetic Analysis of Two Japanese Patients With Non-Classical 21-Hydroxylase Deficiency

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Structural Signature of Classical Versus Late-Onset Friedreich's Ataxia by Multimodality Brain MRI

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