نتائج البحث - Maria I. New
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Male pseudohermaphroditism due to 17α-hydroxylase deficiency حسب Maria I. New
منشور في 1970Artigo -
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Nonclassical 21-Hydroxylase Deficiency حسب Maria I. New
منشور في 2006Revisão -
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A New Form of Congenital Adrenal Hyperplasia<sup>1</sup> حسب Maria I. New, Ralph E. Peterson
منشور في 1967Artigo -
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Structure of human steroid 21-hydroxylase genes. حسب Perrin C. White, Maria I. New, Bo Dupont
منشور في 1986Artigo -
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Addison’s Disease 2001 حسب Svetlana Ten, Maria I. New, Noel K. Maclaren
منشور في 2001Revisão -
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HDAC inhibitor‐based therapies: Can we interpret the code? حسب Maria I. New, Heidi Olzscha, Nicholas B. La Thangue
منشور في 2012Revisão -
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Growth Hormone Therapy Alone or in Combination with Gonadotropin-Releasing Hormone Analog Therapy to Improve the Height Deficit in Children with Congenital Adrenal Hyperplasia<sup>... حسب Jose Bernardo Quintos, Maria G. Vogiatzi, Madeleine D. Harbison, Maria I. New
منشور في 2001Artigo -
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Mutations in Steroid 21-Hydroxylase (CYP21) حسب Perrin C. White, Maria-Teresa Tusie-Luna, Maria I. New, Phyllis Speiser
منشور في 1994Revisão -
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أدوات البحث:
موضوعات ذات صلة
Biology
Medicine
Internal medicine
Endocrinology
Genetics
Congenital adrenal hyperplasia
Gene
Hormone
Biochemistry
Mutation
21-Hydroxylase
Chemistry
Androgen
Molecular biology
Pediatrics
Pregnancy
Allele
Cell biology
Missense mutation
Osteoporosis
Aldosterone
Dexamethasone
Disease
Enzyme
Genotype
Hyperplasia
Luteinizing hormone
Receptor
Fetus
Follicle-stimulating hormone