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Hyperinsulinism in Infancy: From Basic Science to Clinical Disease

Physiological reviews, 2004-01, Vol.84 (1), p.239-275

2004

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Translating research into political advocacy to improve infant and child health

Early human development, 2014-11, Vol.90 (11), p.761-764

Kt, Albert Aynsley-Green

2014

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Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds

Pediatrics (Evanston), 2000-05, Vol.105 (5), p.1141-1145

2000

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The British Betrayal of Childhood: Challenging Uncomfortable Truths and Bringing About Change

Aynsley-Green, Al

1st, 2019

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Glucose Regulates Islet Amyloid Polypeptide Gene Transcription in a PDX1- and Calcium-dependent Manner

The Journal of biological chemistry, 2000-05, Vol.275 (20), p.15330-15335

2000

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Improving the care of children and young people in the UK: 20years on

Archives of disease in childhood, 2015-01, Vol.100 (1), p.4-7

Aynsley-Green, Albert

2015

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Improving the care of children and young people in the UK: 20 years on

Archives of disease in childhood, 2015-01, Vol.100 (1), p.4-7

Aynsley-Green, Albert

2015

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Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion

The Journal of clinical investigation, 2001-08, Vol.108 (3), p.457-465

2001

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Engineering a Glucose-responsive Human Insulin-secreting Cell Line from Islets of Langerhans Isolated from a Patient with Persistent Hyperinsulinemic Hypoglycemia of Infancy

The Journal of biological chemistry, 1999-11, Vol.274 (48), p.34059-34066

1999

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A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

Nature genetics, 2000-09, Vol.26 (1), p.56-60

2000

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Safeguarding children: a call to action

The Lancet (British edition), 2009-01, Vol.373 (9660), p.280-281

2009

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Putting Compassion Back into Care: Focus on Minority Ethnic Families Experiencing Dementia

Sushruta Journal of Health Policy & Opinion, 2023-10, Vol.15 (3)

Aynsley-Green, Albert

2023

Volltextzugriff (PDF)

Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy and Mutations in the Sulfonylurea Receptor

The New England journal of medicine, 1997-03, Vol.336 (10), p.703-706

1997

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Who is speaking for children and adolescents and for their health at the policy level?

BMJ (Online), 2000-07, Vol.321 (7255), p.229-232

International edition, 2000

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Management of hyperinsulinism in infancy and childhood

Annals of medicine (Helsinki), 2000, Vol.32 (8), p.544-551

2000

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The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation

The journal of clinical endocrinology and metabolism, 1991-11, Vol.73 (5), p.969-974

1991

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Hyperinsulinism of infancy : The regulated release of insulin by KATP channel-independent pathways

Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.329-339

2001

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Therapy for persistent hyperinsulinemic hypoglycemia of infancy. Understanding the responsiveness of beta cells to diazoxide and somatostatin

The Journal of clinical investigation, 1997-10, Vol.100 (7), p.1888-1893

1997

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Impaired expression of transcription factor IUF1 in a pancreatic β-cell line derived from a patient with persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis)

FEBS letters, 1997-08, Vol.413 (2), p.304-308

1997

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Genetics and pathophysiology of hyperinsulinism in infancy

Hormone research, 2004-01, Vol.61 (6), p.270-288

2004

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Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p

Journal of Pediatric Endocrinology and Metabolism, 2004-12, Vol.17 (12), p.1613

2004

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Loss of functional K ATP channels in pancreatic β-cells causes persistent hyperinsulinemic hypoglycemia of infancy

Nature medicine, 1996-12, Vol.2 (12), p.1344-1347

1996

Volltextzugriff (PDF)

Sulfonylurea receptor 1 and Kir6.2 expression in the novel human insulin-secreting cell line NES2Y

Diabetes (New York, N.Y.), 2000-06, Vol.49 (6), p.953-960

2000

Volltextzugriff (PDF)

Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI)

Pediatric endocrinology reviews : PER, 2004-11, Vol.2 Suppl 1, p.163

2004

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Nature's KATP-Channel Knockout

Physiology (Bethesda, Md.), 1997-10, Vol.12 (5), p.197-203

1997

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Hyperinsulinism in Infancy: From Basic Science to Clinical Disease

Translating research into political advocacy to improve infant and child health

Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds

The British Betrayal of Childhood: Challenging Uncomfortable Truths and Bringing About Change

Glucose Regulates Islet Amyloid Polypeptide Gene Transcription in a PDX1- and Calcium-dependent Manner

Improving the care of children and young people in the UK: 20years on

Improving the care of children and young people in the UK: 20 years on

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion

Engineering a Glucose-responsive Human Insulin-secreting Cell Line from Islets of Langerhans Isolated from a Patient with Persistent Hyperinsulinemic Hypoglycemia of Infancy

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

Safeguarding children: a call to action

Putting Compassion Back into Care: Focus on Minority Ethnic Families Experiencing Dementia

Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy and Mutations in the Sulfonylurea Receptor

Who is speaking for children and adolescents and for their health at the policy level?

Management of hyperinsulinism in infancy and childhood

The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation

Hyperinsulinism of infancy : The regulated release of insulin by KATP channel-independent pathways

Therapy for persistent hyperinsulinemic hypoglycemia of infancy. Understanding the responsiveness of beta cells to diazoxide and somatostatin

Impaired expression of transcription factor IUF1 in a pancreatic β-cell line derived from a patient with persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis)

Genetics and pathophysiology of hyperinsulinism in infancy

Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p

Loss of functional K ATP channels in pancreatic β-cells causes persistent hyperinsulinemic hypoglycemia of infancy

Sulfonylurea receptor 1 and Kir6.2 expression in the novel human insulin-secreting cell line NES2Y

Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI)

Nature's KATP-Channel Knockout

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