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Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians

Genetics in medicine, 2017-11, Vol.19 (11), p.1276-1279

2017

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Pituitary Tumor Transforming Gene (PTTG) Expression in Pituitary Adenomas

The journal of clinical endocrinology and metabolism, , Vol.84 (2), p.761-767

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Structure, Expression, and Function of Human Pituitary Tumor-Transforming Gene (PTTG)

Molecular endocrinology (Baltimore, Md.), 1999-01, Vol.13 (1), p.156-166

1999

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1349-P: People with Type 2 Diabetes Have a High Prevalence of Nonalcoholic Steatohepatitis with Significant Fibrosis When Screened by NIS4 or Elastography

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

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Combined Cyclic Vomiting and Kearns-Sayre Syndromes

Pediatric neurology, 2007-02, Vol.36 (2), p.135-136

2007

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Molecular Characterization of the Men1 Tumor Suppressor Gene in Sporadic Pituitary Tumors

The journal of clinical endocrinology and metabolism, 1998-04, Vol.83 (4), p.1388-1391

1998

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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

Nature genetics, 1993-07, Vol.4 (3), p.289-294

1993

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An Intronless Homolog of Human Proto-Oncogene hPTTG Is Expressed in Pituitary Tumors: Evidence for hPTTG Family

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.1149-1152

1999

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Isolated familial somatotropinomas: clinical features and analysis of the MEN1 gene

Pituitary, 2002-01, Vol.5 (1), p.11-15

2002

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Long-acting peptidomimergic control of gigantism caused by pituitary acidophilic stem cell adenoma

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3409-3416

2000

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Identification of an overexpressed yeast gene which prevents aminoglycoside toxicity

Microbiology (Society for General Microbiology), 1996-12, Vol.142 ( Pt 12), p.3407

1996

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Loss of heterozygosity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the multiple endocrine neoplasia type I gene

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (1), p.249-256

1999

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Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome

Pediatric research, 1992-06, Vol.31 (6), p.557-560

1992

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Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity

American journal of otolaryngology, 1997-05, Vol.18 (3), p.173-178

1997

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Molecular pathogenesis of pituitary disorders

Current opinion in endocrinology & diabetes, 2002-02, Vol.9 (1), p.61-78

2002

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Mitochondrial mutation associated with nonsyndromic deafness

American journal of otolaryngology, 1995-11, Vol.16 (6), p.403-408

1995

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Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

American journal of otolaryngology, 1993-11, Vol.14 (6), p.399-403

1993

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Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome

The Journal of pediatrics, 1993-10, Vol.123 (4), p.598-602

1993

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Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness

Pharmacogenetics (London), 1995-06, Vol.5 (3), p.165-172

1995

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Long-Acting Peptidomimergic Control of Gigantism Caused by Pituitary Acidophilic Stem Cell Adenoma1

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3409-3416

2000

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Long-Acting Peptidomimergic Control of Gigantism Caused by Pituitary Acidophilic Stem Cell Adenoma

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3409-3416

2000

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Loss of Heterozygosity on Chromosome 11q13 in Two Families with Acromegaly/Gigantism Is Independent of Mutations of the Multiple Endocrine Neoplasia Type I Gene1

The journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.249-256

1999

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Loss of Heterozygosity on Chromosome 11q13 in Two Families with Acromegaly/Gigantism Is Independent of Mutations of the Multiple Endocrine Neoplasia Type I Gene 1

The journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.249-256

1999

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Expression of human lysosomal β-hexosaminidase in yeast vacuoles

Biochemical and biophysical research communications, 1990-07, Vol.170 (1), p.383-390

Prezant, Toni R.

1990

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Corrections to the human mitochondrial ribosomal RNA sequences

Human genetics, 1994, Vol.93 (1), p.87-88

1994

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Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians

Pituitary Tumor Transforming Gene (PTTG) Expression in Pituitary Adenomas

Structure, Expression, and Function of Human Pituitary Tumor-Transforming Gene (PTTG)

1349-P: People with Type 2 Diabetes Have a High Prevalence of Nonalcoholic Steatohepatitis with Significant Fibrosis When Screened by NIS4 or Elastography

Combined Cyclic Vomiting and Kearns-Sayre Syndromes

Molecular Characterization of the Men1 Tumor Suppressor Gene in Sporadic Pituitary Tumors

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

An Intronless Homolog of Human Proto-Oncogene hPTTG Is Expressed in Pituitary Tumors: Evidence for hPTTG Family

Isolated familial somatotropinomas: clinical features and analysis of the MEN1 gene

Long-acting peptidomimergic control of gigantism caused by pituitary acidophilic stem cell adenoma

Identification of an overexpressed yeast gene which prevents aminoglycoside toxicity

Loss of heterozygosity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the multiple endocrine neoplasia type I gene

Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity

Molecular pathogenesis of pituitary disorders

Mitochondrial mutation associated with nonsyndromic deafness

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome

Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness

Long-Acting Peptidomimergic Control of Gigantism Caused by Pituitary Acidophilic Stem Cell Adenoma1

Long-Acting Peptidomimergic Control of Gigantism Caused by Pituitary Acidophilic Stem Cell Adenoma

Loss of Heterozygosity on Chromosome 11q13 in Two Families with Acromegaly/Gigantism Is Independent of Mutations of the Multiple Endocrine Neoplasia Type I Gene1

Loss of Heterozygosity on Chromosome 11q13 in Two Families with Acromegaly/Gigantism Is Independent of Mutations of the Multiple Endocrine Neoplasia Type I Gene 1

Expression of human lysosomal β-hexosaminidase in yeast vacuoles

Corrections to the human mitochondrial ribosomal RNA sequences

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