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1

Male pseudohermaphroditism due to 17α-hydroxylase deficiency -н Maria I. New

Хэвлэсэн 1970

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2

Nonclassical 21-Hydroxylase Deficiency -н Maria I. New

Хэвлэсэн 2006

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3

Genotype and Hormonal Phenotype in Nonclassical 21-Hydroxylase Deficiency* -н Phyllis Speiser, Maria I. New

Хэвлэсэн 1987

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4

A New Form of Congenital Adrenal Hyperplasia1 -н Maria I. New, Ralph E. Peterson

Хэвлэсэн 1967

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5

Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess -н Maria I. New, Robert C. Wilson

Хэвлэсэн 1999

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6

Structure of human steroid 21-hydroxylase genes. -н Perrin C. White, Maria I. New, Bo Dupont

Хэвлэсэн 1986

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7

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation. -н Perrin C. White, Maria I. New, B Dupont

Хэвлэсэн 1984

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8

Long Term Outcome in Adult Males with Classic Congenital Adrenal Hyperplasia1 -н Monina S. Cabrera, Maria G. Vogiatzi, Maria I. New

Хэвлэсэн 2001

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9

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. -н Perrin C. White, Maria I. New, Bo Dupont

Хэвлэсэн 1984

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10

Addison’s Disease 2001 -н Svetlana Ten, Maria I. New, Noel K. Maclaren

Хэвлэсэн 2001

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11

Aldosterone excretion in normal children and in children with adrenal hyperplasia. -н Maria I. New, Barbara Stoler Miller, Ralph E. Peterson

Хэвлэсэн 1966

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12

HDAC inhibitor‐based therapies: Can we interpret the code? -н Maria I. New, Heidi Olzscha, Nicholas B. La Thangue

Хэвлэсэн 2012

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13

The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency -н Minu George, Maria I. New, Svetlana Ten, Charles Sultan, Amrit Bhangoo

Хэвлэсэн 2010

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14

Fertility in patients with congenital adrenal hyperplasia -н David E. Reichman, Perrin C. White, Maria I. New, Zev Rosenwaks

Хэвлэсэн 2013

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15

Genetic Defects of Steroidogenesis in Premature Pubarche* -н JEAN W. TEMECK, Songya Pang, Christopher P. Nelson, Maria I. New

Хэвлэсэн 1987

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16

Growth Hormone Therapy Alone or in Combination with Gonadotropin-Releasing Hormone Analog Therapy to Improve the Height Deficit in Children with Congenital Adrenal Hyperplasia... -н Jose Bernardo Quintos, Maria G. Vogiatzi, Madeleine D. Harbison, Maria I. New

Хэвлэсэн 2001

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17

Mutations in Steroid 21-Hydroxylase (CYP21) -н Perrin C. White, Maria-Teresa Tusie-Luna, Maria I. New, Phyllis Speiser

Хэвлэсэн 1994

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18

Aldosterone Synthesis in Salt-Wasting Congenital Adrenal Hyperplasia with Complete Absence of Adrenal 21-Hydroxylase -н Phyllis Speiser, Levon Agdere, Hajime Ueshiba, Perrin C. White, Maria I. New

Хэвлэсэн 1991

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19

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. -н M Amor, K L Parker, Hadas Globerman, Maria I. New, Perrin C. White

Хэвлэсэн 1988

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20

Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: Results of a pilot study -н Paul D. Trautman, Heino F. L. Meyer‐Bahlburg, Jill Postelnek, Maria I. New

Хэвлэсэн 1995

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Male pseudohermaphroditism due to 17α-hydroxylase deficiency -н Maria I. New

Nonclassical 21-Hydroxylase Deficiency -н Maria I. New

Genotype and Hormonal Phenotype in Nonclassical 21-Hydroxylase Deficiency* -н Phyllis Speiser, Maria I. New

A New Form of Congenital Adrenal Hyperplasia<sup>1</sup> -н Maria I. New, Ralph E. Peterson

Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess -н Maria I. New, Robert C. Wilson

Structure of human steroid 21-hydroxylase genes. -н Perrin C. White, Maria I. New, Bo Dupont

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation. -н Perrin C. White, Maria I. New, B Dupont

Long Term Outcome in Adult Males with Classic Congenital Adrenal Hyperplasia<sup>1</sup> -н Monina S. Cabrera, Maria G. Vogiatzi, Maria I. New

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. -н Perrin C. White, Maria I. New, Bo Dupont

Addison’s Disease 2001 -н Svetlana Ten, Maria I. New, Noel K. Maclaren

Aldosterone excretion in normal children and in children with adrenal hyperplasia. -н Maria I. New, Barbara Stoler Miller, Ralph E. Peterson

HDAC inhibitor‐based therapies: Can we interpret the code? -н Maria I. New, Heidi Olzscha, Nicholas B. La Thangue

The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency -н Minu George, Maria I. New, Svetlana Ten, Charles Sultan, Amrit Bhangoo

Fertility in patients with congenital adrenal hyperplasia -н David E. Reichman, Perrin C. White, Maria I. New, Zev Rosenwaks

Genetic Defects of Steroidogenesis in Premature Pubarche* -н JEAN W. TEMECK, Songya Pang, Christopher P. Nelson, Maria I. New

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>... -н Jose Bernardo Quintos, Maria G. Vogiatzi, Madeleine D. Harbison, Maria I. New

Mutations in Steroid 21-Hydroxylase (CYP21) -н Perrin C. White, Maria-Teresa Tusie-Luna, Maria I. New, Phyllis Speiser

Aldosterone Synthesis in Salt-Wasting Congenital Adrenal Hyperplasia with Complete Absence of Adrenal 21-Hydroxylase -н Phyllis Speiser, Levon Agdere, Hajime Ueshiba, Perrin C. White, Maria I. New

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. -н M Amor, K L Parker, Hadas Globerman, Maria I. New, Perrin C. White

Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: Results of a pilot study -н Paul D. Trautman, Heino F. L. Meyer‐Bahlburg, Jill Postelnek, Maria I. New

Хайлтын үр дүнгүүд - Maria I. New

Male pseudohermaphroditism due to 17α-hydroxylase deficiency -н Maria I. New

Nonclassical 21-Hydroxylase Deficiency -н Maria I. New

Genotype and Hormonal Phenotype in Nonclassical 21-Hydroxylase Deficiency* -н Phyllis Speiser, Maria I. New

A New Form of Congenital Adrenal Hyperplasia<sup>1</sup> -н Maria I. New, Ralph E. Peterson

Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess -н Maria I. New, Robert C. Wilson

Structure of human steroid 21-hydroxylase genes. -н Perrin C. White, Maria I. New, Bo Dupont

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation. -н Perrin C. White, Maria I. New, B Dupont

Long Term Outcome in Adult Males with Classic Congenital Adrenal Hyperplasia<sup>1</sup> -н Monina S. Cabrera, Maria G. Vogiatzi, Maria I. New

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. -н Perrin C. White, Maria I. New, Bo Dupont

Addison’s Disease 2001 -н Svetlana Ten, Maria I. New, Noel K. Maclaren

Aldosterone excretion in normal children and in children with adrenal hyperplasia. -н Maria I. New, Barbara Stoler Miller, Ralph E. Peterson

HDAC inhibitor‐based therapies: Can we interpret the code? -н Maria I. New, Heidi Olzscha, Nicholas B. La Thangue

The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency -н Minu George, Maria I. New, Svetlana Ten, Charles Sultan, Amrit Bhangoo

Fertility in patients with congenital adrenal hyperplasia -н David E. Reichman, Perrin C. White, Maria I. New, Zev Rosenwaks

Genetic Defects of Steroidogenesis in Premature Pubarche* -н JEAN W. TEMECK, Songya Pang, Christopher P. Nelson, Maria I. New

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>... -н Jose Bernardo Quintos, Maria G. Vogiatzi, Madeleine D. Harbison, Maria I. New

Mutations in Steroid 21-Hydroxylase (CYP21) -н Perrin C. White, Maria-Teresa Tusie-Luna, Maria I. New, Phyllis Speiser

Aldosterone Synthesis in Salt-Wasting Congenital Adrenal Hyperplasia with Complete Absence of Adrenal 21-Hydroxylase -н Phyllis Speiser, Levon Agdere, Hajime Ueshiba, Perrin C. White, Maria I. New

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. -н M Amor, K L Parker, Hadas Globerman, Maria I. New, Perrin C. White

Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: Results of a pilot study -н Paul D. Trautman, Heino F. L. Meyer‐Bahlburg, Jill Postelnek, Maria I. New

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