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Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism

The journal of clinical endocrinology and metabolism, 2013-02, Vol.98 (2), p.E355-E363

2013

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Recycling endosome-dependent and -independent mechanisms for IL-10 secretion in LPS-activated macrophages

Journal of leukocyte biology, 2012-12, Vol.92 (6), p.1227-1239

2012

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Intranasal immunisation with Toxoplasma gondii tachyzoite antigen encapsulated into PLG microspheres induces humoral and cell-mediated immunity in sheep

Vaccine, 2004-09, Vol.22 (29), p.3929-3941

2004

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Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene

The New England journal of medicine, 1998-05, Vol.338 (19), p.1352-1357

1998

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Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation

The New England journal of medicine, 1998-01, Vol.338 (4), p.226-230

1998

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HYPERINSULINISM IN INFANTS AND CHILDREN

The Pediatric clinics of North America, 1997-04, Vol.44 (2), p.363-374

Stanley, Charles A.

1997

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The Causes of Neonatal Hypoglycemia

The New England journal of medicine, 1999-04, Vol.340 (15), p.1200-1201

1999

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Diamond-based structures to collect and guide light

New journal of physics, 2011-02, Vol.13 (2), p.025020

2011

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Strongly enhanced photon collection from diamond defect centers under microfabricated integrated solid immersion lenses

Applied physics letters, 2010-12, Vol.97 (24)

2010

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Genetic Heterogeneity in Familial Hyperinsulinism

Human molecular genetics, 1998-07, Vol.7 (7), p.1119-1128

1998

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Dysregulation of Insulin Secretion in Children With Congenital Hyperinsulinism due to Sulfonylurea Receptor Mutations

Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.322-328

2001

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Parsing ketotic hypoglycaemia

Archives of disease in childhood, 2006-06, Vol.91 (6), p.460-461

Stanley, C A

2006

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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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The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic condition

Clinical genetics, 2006-06, Vol.69 (6), p.486-496

2006

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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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In the Literature

Clinical infectious diseases, 2024-10, Vol.79 (4), p.i-iv

Deresinski, Stanley C

2024

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In the Literature

Clinical infectious diseases, 2024-09, Vol.79 (3), p.i-iii

Deresinski, Stanley C

2024

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Nanofabricated solid immersion lenses registered to single emitters in diamond

Applied physics letters, 2011-03, Vol.98 (13), p.133107-133107-3

2011

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In the Literature

Clinical infectious diseases, 2024-07, Vol.79 (1), p.i-iii

Deresinski, Stanley C

2024

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In the Literature

Clinical infectious diseases, 2024-04, Vol.78 (4), p.i-iii

Deresinski, Stanley C

2024

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A syndrome of congenital hyperinsulinism and hyperammonemia

The Journal of pediatrics, 1997-04, Vol.130 (4), p.661-664

1997

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In the Literature

Clinical infectious diseases, 2024-03, Vol.78 (3), p.i-iv

Deresinski, Stanley C

2024

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In the Literature

Clinical infectious diseases, 2024-02, Vol.78 (2), p.i-iv

Deresinski, Stanley C

2024

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IN THE LITERATURE

Clinical infectious diseases, 2024-01, Vol.78 (1), p.i-iv

Deresinski, Stanley C

2024

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In the Literature

Clinical infectious diseases, 2023-12, Vol.77 (12), p.i-ii

Deresinski, Stanley C

2023

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Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism

Recycling endosome-dependent and -independent mechanisms for IL-10 secretion in LPS-activated macrophages

Intranasal immunisation with Toxoplasma gondii tachyzoite antigen encapsulated into PLG microspheres induces humoral and cell-mediated immunity in sheep

Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene

Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation

HYPERINSULINISM IN INFANTS AND CHILDREN

The Causes of Neonatal Hypoglycemia

Diamond-based structures to collect and guide light

Strongly enhanced photon collection from diamond defect centers under microfabricated integrated solid immersion lenses

Genetic Heterogeneity in Familial Hyperinsulinism

Dysregulation of Insulin Secretion in Children With Congenital Hyperinsulinism due to Sulfonylurea Receptor Mutations

Parsing ketotic hypoglycaemia

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

The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic condition

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

In the Literature

In the Literature

Nanofabricated solid immersion lenses registered to single emitters in diamond

In the Literature

In the Literature

A syndrome of congenital hyperinsulinism and hyperammonemia

In the Literature

In the Literature

IN THE LITERATURE

In the Literature

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