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Emerging epidemic of type 2 diabetes in youth

Diabetes care, 1999-02, Vol.22 (2), p.345-354

1999

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Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (1), p.50-57

1999

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Intracerebral crises during treatment of diabetic ketoacidosis

Diabetes care, 1990-01, Vol.13 (1), p.22-33

Rosenbloom, A L

1990

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Growth hormone insensitivity: Physiologic and genetic basis, phenotype, and treatment

The Journal of pediatrics, 1999-09, Vol.135 (3), p.280-289

Rosenbloom, Arlan L.

1999

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Growth hormone receptor deficiency in ecuador

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4436-4443

1999

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Is short stature a handicap? A comparison of the psychosocial functioning of referred and nonreferred children with normal short stature and children with normal stature

The Journal of pediatrics, 2000, Vol.136 (1), p.96-102

2000

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Two-year treatment of growth hormone (GH) receptor deficiency with recombinant insulin-like growth factor I in 22 children : Comparison of two dosage levels and to GH-treated GH deficiency

The Journal of clinical endocrinology and metabolism, 1997-02, Vol.82 (2), p.629-633

1997

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Stature in ecuadorians heterozygous for growth hormone receptor gene E180 splice mutation does not differ from that of homozygous normal relatives

The journal of clinical endocrinology and metabolism, 1998-07, Vol.83 (7), p.2373-2375

1998

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Long-term glycemic control influences the onset of limited joint mobility in type 1 diabetes

The Journal of pediatrics, 1998-06, Vol.132 (6), p.944-947

1998

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CONNECTIVE TISSUE AND JOINT DISEASE IN DIABETES MELLITUS

Endocrinology and metabolism clinics of North America, 1996-06, Vol.25 (2), p.473-483

1996

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Treatment of type 2 diabetes mellitus in children and adolescents

Journal of pediatric endocrinology & metabolism : JPEM, 2000-12, Vol.13 Suppl 6, p.1403

2000

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Bone Mineral, Histomorphometry, and Body Composition in Adults with Growth Hormone Receptor Deficiency

Journal of bone and mineral research, 1998-03, Vol.13 (3), p.415-421

1998

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Normal intelligence with severe insulin-like growth factor I deficiency due to growth hormone receptor deficiency : A controlled study in a genetically homogeneous population

The journal of clinical endocrinology and metabolism, 1998-06, Vol.83 (6), p.1953-1958

1998

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A mathematical model for predicting growth response to growth hormone replacement therapy--a useful clinical tool or an intellectual exercise?

The journal of clinical endocrinology and metabolism, 1999-04, Vol.84 (4), p.1172-1173

Rosenbloom, A L

1999

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Diabetic Ketoacidosis (DKA): Treatment Guidelines

Clinical pediatrics, 1996-05, Vol.35 (5), p.261-266

1996

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Misuse of Tanner puberty stages to estimate chronologic age

Pediatrics (Evanston), 1998-12, Vol.102 (6), p.1494-1494

1998

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Lessons from the Genetics of Laron Syndrome

Trends in endocrinology and metabolism, 1998-09, Vol.9 (7), p.276-283

1998

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Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type lb and the associated methylation defect at exon A/B: Evidence for a long-range regulatory element within the imprinted GNAS1 locus

Human molecular genetics, 2001-06, Vol.10 (12), p.1231-1241

2001

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Why Diabetes Camp?

Clinical pediatrics, 2001-09, Vol.40 (9), p.511-516

Rosenbloom, Arlan L.

2001

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Diabetic ketoacidosis and hyperglycemic hyperosmolar state

Pediatric diabetes, 2014-09, Vol.15 (S20), p.154-179

2014

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Hormonal and metabolic effects and pharmacokinetics of recombinant insulin-like growth factor-I in growth hormone receptor deficiency/Laron syndrome

The journal of clinical endocrinology and metabolism, 1993-07, Vol.77 (1), p.273-280

1993

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The composition and distribution of insulin-like growth factors (IGFs) and IGF-binding proteins (IGFBPs) in the serum of growth hormone receptor-deficient patients : effects of IGF-I therapy on IGFBP-3

The journal of clinical endocrinology and metabolism, 1993-12, Vol.77 (6), p.1683-1689

1993

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Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1 locus

Human molecular genetics, 2001-06, Vol.10 (12), p.1231-1241

2001

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GROWTH HORMONE INSENSITIVITY

The Pediatric clinics of North America, 1997-04, Vol.44 (2), p.423-442

1997

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Psychosocial aspects of short stature and growth hormone therapy

The Journal of pediatrics, 1999-07, Vol.135 (1), p.133-134

1999

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Emerging epidemic of type 2 diabetes in youth

Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene

Intracerebral crises during treatment of diabetic ketoacidosis

Growth hormone insensitivity: Physiologic and genetic basis, phenotype, and treatment

Growth hormone receptor deficiency in ecuador

Is short stature a handicap? A comparison of the psychosocial functioning of referred and nonreferred children with normal short stature and children with normal stature

Two-year treatment of growth hormone (GH) receptor deficiency with recombinant insulin-like growth factor I in 22 children : Comparison of two dosage levels and to GH-treated GH deficiency

Stature in ecuadorians heterozygous for growth hormone receptor gene E180 splice mutation does not differ from that of homozygous normal relatives

Long-term glycemic control influences the onset of limited joint mobility in type 1 diabetes

CONNECTIVE TISSUE AND JOINT DISEASE IN DIABETES MELLITUS

Treatment of type 2 diabetes mellitus in children and adolescents

Bone Mineral, Histomorphometry, and Body Composition in Adults with Growth Hormone Receptor Deficiency

Normal intelligence with severe insulin-like growth factor I deficiency due to growth hormone receptor deficiency : A controlled study in a genetically homogeneous population

A mathematical model for predicting growth response to growth hormone replacement therapy--a useful clinical tool or an intellectual exercise?

Diabetic Ketoacidosis (DKA): Treatment Guidelines

Misuse of Tanner puberty stages to estimate chronologic age

Lessons from the Genetics of Laron Syndrome

Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type lb and the associated methylation defect at exon A/B: Evidence for a long-range regulatory element within the imprinted GNAS1 locus

Why Diabetes Camp?

Diabetic ketoacidosis and hyperglycemic hyperosmolar state

Hormonal and metabolic effects and pharmacokinetics of recombinant insulin-like growth factor-I in growth hormone receptor deficiency/Laron syndrome

The composition and distribution of insulin-like growth factors (IGFs) and IGF-binding proteins (IGFBPs) in the serum of growth hormone receptor-deficient patients : effects of IGF-I therapy on IGFBP-3

Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1 locus

GROWTH HORMONE INSENSITIVITY

Psychosocial aspects of short stature and growth hormone therapy

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