X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation

L. Angelova,; E. Michaylova,; E. Stephanova,; M. Ivanova,; Β. Molzer,; I. Kremensky,

doi:10.1515/IJDHD.2001.2.4.247

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X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation

L. Angelova, , E. Michaylova, , E. Stephanova, , M. Ivanova, , Β. Molzer, und I. Kremensky,

Veröffentlicht/Copyright: 1. Oktober 2001

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Aus der Zeitschrift International Journal on Disability and Human Development Band 2 Heft 4

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Angelova,, L., Michaylova,, E., Stephanova,, E., Ivanova,, M., Molzer,, Β. and Kremensky,, I.. "X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation" International Journal on Disability and Human Development, vol. 2, no. 4, pp. 247-250. https://doi.org/10.1515/IJDHD.2001.2.4.247

Angelova,, L., Michaylova,, E., Stephanova,, E., Ivanova,, M., Molzer,, Β. & Kremensky,, I. (). X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation. International Journal on Disability and Human Development, 2(4), 247-250. https://doi.org/10.1515/IJDHD.2001.2.4.247

Angelova,, L., Michaylova,, E., Stephanova,, E., Ivanova,, M., Molzer,, Β. and Kremensky,, I. () X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation. International Journal on Disability and Human Development, Vol. 2 (Issue 4), pp. 247-250. https://doi.org/10.1515/IJDHD.2001.2.4.247

Angelova,, L., Michaylova,, E., Stephanova,, E., Ivanova,, M., Molzer,, Β. and Kremensky,, I.. "X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation" International Journal on Disability and Human Development 2, no. 4 (): 247-250. https://doi.org/10.1515/IJDHD.2001.2.4.247

Angelova, L, Michaylova, E, Stephanova, E, Ivanova, M, Molzer, Β, Kremensky, I. X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation. International Journal on Disability and Human Development. ;2(4): 247-250. https://doi.org/10.1515/IJDHD.2001.2.4.247

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Published Online: 2001-10

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Artikel in diesem Heft

CONTENTS
Letter from the Editors
Molecular Genetics of Thyroid Disorders in the Neonate: A Review
Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
Adrenal Mass in Carney Triad
An Infrequent Double Mutation in the MEN1 Gene
X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation
BOOK REVIEWS. CALENDAR. INDEX

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https://doi.org/10.1515/IJDHD.2001.2.4.247

Artikel in diesem Heft

CONTENTS
Letter from the Editors
Molecular Genetics of Thyroid Disorders in the Neonate: A Review
Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
Adrenal Mass in Carney Triad
An Infrequent Double Mutation in the MEN1 Gene
X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation
BOOK REVIEWS. CALENDAR. INDEX