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Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

The journal of clinical endocrinology and metabolism, 2004-12, Vol.89 (12), p.6224-6234

2004

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Treatment of Congenital Hyperinsulinism with Lanreotide Acetate (Somatuline Autogel)

The journal of clinical endocrinology and metabolism, 2011-08, Vol.96 (8), p.2312-2317

2011

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Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy

The Journal of pediatrics, 1993-10, Vol.123 (4), p.644-650

1993

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Surgical versus non-surgical treatment of congenital hyperinsulinism

Pediatric endocrinology reviews : PER, 2009-03, Vol.6 (3), p.424

2009

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ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia

Genetics in medicine, 2011-10, Vol.13 (10), p.891-894

2011

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Cognitive and developmental outcome of conservatively treated children with congenital hyperinsulinism

Journal of Pediatric Endocrinology and Metabolism, 2013, Vol.26 (3-4), p.301-308

2013

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Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War

Pediatric diabetes, 2012-06, Vol.13 (4), p.326-333

2012

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A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

Diabetes (New York, N.Y.), 1997-11, Vol.46 (11), p.1743-1748

1997

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Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi Jews

Human molecular genetics, 1996-11, Vol.5 (11), p.1813-1822

1996

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Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene

Diabetes (New York, N.Y.), 1999-08, Vol.48 (8), p.1652-1657

1999

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Hyperinsulinemic hypoglycemia of infancy (Nesidioblstosis) in clinical remission : high incidence of diabetes mellitus and persistent β-cell dysfunction at long-term follow-up

The journal of clinical endocrinology and metabolism, 1995-02, Vol.80 (2), p.386-392

1995

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Neonatal Hyperinsulinism

Trends in Endocrinology & Metabolism, 1999-03, Vol.10 (2), p.55-61

1999

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Predictors of growth response to growth hormone in otherwise normal short children

The Journal of pediatrics, 1992-07, Vol.121 (1), p.44-48

1992

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Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism

Human mutation, 1999, Vol.14 (1), p.23-29

1999

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Final height after growth hormone therapy in peripubertal boys with a subnormal integrated concentration of growth hormone

Hormone research, 1992-01, Vol.37 (4-5), p.150-155

1992

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Assessment of growth hormone (GH) axis in turner's syndrome using 24-hour integrated concentrations of GH, insulin-like growth factor-I, plasma GH-binding activity, GH binding to IM9 cells, and GH response to pharmacological stimulation

The journal of clinical endocrinology and metabolism, 1992-08, Vol.75 (2), p.412-416

1992

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Parathyroid adenoma after radiation in an 8-year-old boy

The Journal of pediatrics, 1998-05, Vol.132 (5), p.892-893

1998

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Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

Human molecular genetics, 1995-05, Vol.4 (5), p.879-886

1995

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PERSISTENT HYPERINSULINAEMIC HYPOGLYCAEMIA OF INFANCY: LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOGUE SANDOSTATIN

Clinical endocrinology (Oxford), 1989-07, Vol.31 (1), p.71-80

1989

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Age as a determinant of the impact of growth hormone therapy on predicted adult height

Clinical endocrinology (Oxford), 1994-09, Vol.41 (3), p.331-335

1994

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Precocious Puberty in Myelomeningocele Patients

Journal of pediatric orthopaedics, 1984-01, Vol.4 (1), p.28-31

1984

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Effect of timing of growth hormone administration on plasma growth-hormone-binding activity, insulin-like growth factor-I and growth in children with a subnormal spontaneous secretion of growth hormone

Hormone research, 1993-01, Vol.39 (5-6), p.188-191

1993

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Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

Human molecular genetics, 1995-11, Vol.4 (11), p.2187-2188

1995

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Who Will Benefit from Growth Hormone Therapy? Growth Hormone Therapy in Short Children

Journal of Pediatric Endocrinology and Metabolism, 1992-01, Vol.5 (1-2)

1992

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Neurobehavioral profile of children with persistent hyperinsulinemic hypoglycemia of infancy

Developmental neuropsychology, 1994-01, Vol.10 (2), p.153-163

1994

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Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

Treatment of Congenital Hyperinsulinism with Lanreotide Acetate (Somatuline Autogel)

Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy

Surgical versus non-surgical treatment of congenital hyperinsulinism

ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia

Cognitive and developmental outcome of conservatively treated children with congenital hyperinsulinism

Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi Jews

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene

Hyperinsulinemic hypoglycemia of infancy (Nesidioblstosis) in clinical remission : high incidence of diabetes mellitus and persistent β-cell dysfunction at long-term follow-up

Neonatal Hyperinsulinism

Predictors of growth response to growth hormone in otherwise normal short children

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism

Final height after growth hormone therapy in peripubertal boys with a subnormal integrated concentration of growth hormone

Assessment of growth hormone (GH) axis in turner's syndrome using 24-hour integrated concentrations of GH, insulin-like growth factor-I, plasma GH-binding activity, GH binding to IM9 cells, and GH response to pharmacological stimulation

Parathyroid adenoma after radiation in an 8-year-old boy

Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

PERSISTENT HYPERINSULINAEMIC HYPOGLYCAEMIA OF INFANCY: LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOGUE SANDOSTATIN

Age as a determinant of the impact of growth hormone therapy on predicted adult height

Precocious Puberty in Myelomeningocele Patients

Effect of timing of growth hormone administration on plasma growth-hormone-binding activity, insulin-like growth factor-I and growth in children with a subnormal spontaneous secretion of growth hormone

Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

Who Will Benefit from Growth Hormone Therapy? Growth Hormone Therapy in Short Children

Neurobehavioral profile of children with persistent hyperinsulinemic hypoglycemia of infancy

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