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Avidity-dependent programming of autoreactive T cells in T1D

PloS one, 2014-05, Vol.9 (5), p.e98074-e98074

2014

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Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers

Nature genetics, 2015-04, Vol.47 (4), p.381-386

2015

Volltextzugriff (PDF)

Antibody Response to Serpin B13 Induces Adaptive Changes in Mouse Pancreatic Islets and Slows Down the Decline in the Residual Beta Cell Function in Children with Recent Onset of Type 1 Diabetes Mellitus

The Journal of biological chemistry, 2016-01, Vol.291 (1), p.266-278

2016

Volltextzugriff (PDF)

Uncoupling of Proliferation and Cytokines From Suppression Within the CD4+CD25+Foxp3+ T―Cell Compartment in the 1st Year of Human Type 1 Diabetes

Diabetes (New York, N.Y.), 2011-08, Vol.60 (8), p.2125-2133

2011

Volltextzugriff (PDF)

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Nature genetics, 2012-01, Vol.44 (1), p.3-5

2012

Volltextzugriff (PDF)

OR.2. Progressive Loss of Regulatory T Cell Function from Diagnosis in Children with Type 1 Diabetes

Clinical immunology (Orlando, Fla.), 2009, Vol.131, p.S6-S6

2009

Volltextzugriff (PDF)

Continuous subcutaneous insulin infusion in toddlers and children with type 1 diabetes mellitus is safe and effective

Pediatric diabetes, 2005-03, Vol.6 (1), p.17-21

2005

Volltextzugriff (PDF)

Growth hormone deficiency and HIV infection

The Journal of pediatrics, 2005-10, Vol.147 (4), p.559-560

2005

Volltextzugriff (PDF)

Avidity-Dependent Programming of Autoreactive T Cells in T1D: e98074

PloS one, 2014-05, Vol.9 (5)

2014

Volltextzugriff (PDF)

Deletion of Lysine 121 Creates a Temperature-sensitive Alteration in Insulin Binding by the Insulin Receptor (∗)

The Journal of biological chemistry, 1995-01, Vol.270 (1), p.476-482

1995

Volltextzugriff (PDF)

Designing and implementing sample and data collection for an international genetics study: the Type 1 Diabetes Genetics Consortium (T1DGC)

Clinical trials (London, England), 2010-08, Vol.7 (1_suppl), p.S5-S32

2010

Volltextzugriff (PDF)

Comprehensive Assessment of Professional Competence: The Rochester Experiment

Teaching and learning in medicine, 2004, Vol.16 (2), p.186-196

2004

Volltextzugriff (PDF)

Hermaphroditus in Greco-Roman myth: lessons and hypotheses for intersex today

Journal of pediatric endocrinology & metabolism : JPEM, 2004-11, Vol.17 (11), p.1471

2004

Volltextzugriff (PDF)

Homozygous nonsense mutation in the insulin receptor gene of a patient with severe congenital insulin resistance: leprechaunism and the role of the insulin-like growth factor receptor

Clinical endocrinology (Oxford), 1996-08, Vol.45 (2), p.229-235

1996

Volltextzugriff (PDF)

Diabetes Mellitus Type 1

Pediatric Clinical Advisor, p.163-164

Jospe, Nicholas

Volltextzugriff (PDF)

Ambiguity of the External Genitalia

Pediatric Clinical Advisor, p.21-22

Jospe, Nicholas

Volltextzugriff (PDF)

Diabetes Mellitus Type 2

Pediatric Clinical Advisor, p.165-166

Jospe, Nicholas

Volltextzugriff (PDF)

Fluids and electrolytes--clinical aspects

Pediatrics in review, 1996-11, Vol.17 (11), p.395

1996

Volltextzugriff (PDF)

Chapter 154 - Disorders of the Adrenal Glands

Pediatrics, p.1032-1039

Jospe, Nicholas

Volltextzugriff (PDF)

Chapter 151 - Disorders of Pubertal Development

Pediatrics, p.1017-1023

Jospe, Nicholas

Volltextzugriff (PDF)

Chapter 152 - Disorders of Sexual Differentiation

Pediatrics, p.1023-1025

Jospe, Nicholas

Volltextzugriff (PDF)

Deletion of 3 basepairs resulting in the loss of lysine-121 in the insulin receptor alpha-subunit in a patient with leprechaunism: binding, phosphorylation, and biological activity

The journal of clinical endocrinology and metabolism, 1994-11, Vol.79 (5), p.1294-1302

1994

Volltextzugriff (PDF)

Melanocytic Nevi in Turner Syndrome

Pediatric dermatology, 1994-06, Vol.11 (2), p.120-124

1994

Volltextzugriff (PDF)

Growth hormone deficiency in an 8-year-old girl with human immunodeficiency virus infection

Pediatrics (Evanston), 1990-08, Vol.86 (2), p.309

1990

Volltextzugriff (PDF)

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

The journal of clinical endocrinology and metabolism, 1986-05, Vol.62 (5), p.995-1002

1986

Volltextzugriff (PDF)

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Avidity-dependent programming of autoreactive T cells in T1D

Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers

Antibody Response to Serpin B13 Induces Adaptive Changes in Mouse Pancreatic Islets and Slows Down the Decline in the Residual Beta Cell Function in Children with Recent Onset of Type 1 Diabetes Mellitus

Uncoupling of Proliferation and Cytokines From Suppression Within the CD4+CD25+Foxp3+ T―Cell Compartment in the 1st Year of Human Type 1 Diabetes

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

OR.2. Progressive Loss of Regulatory T Cell Function from Diagnosis in Children with Type 1 Diabetes

Continuous subcutaneous insulin infusion in toddlers and children with type 1 diabetes mellitus is safe and effective

Growth hormone deficiency and HIV infection

Avidity-Dependent Programming of Autoreactive T Cells in T1D: e98074

Deletion of Lysine 121 Creates a Temperature-sensitive Alteration in Insulin Binding by the Insulin Receptor (∗)

Designing and implementing sample and data collection for an international genetics study: the Type 1 Diabetes Genetics Consortium (T1DGC)

Comprehensive Assessment of Professional Competence: The Rochester Experiment

Hermaphroditus in Greco-Roman myth: lessons and hypotheses for intersex today

Homozygous nonsense mutation in the insulin receptor gene of a patient with severe congenital insulin resistance: leprechaunism and the role of the insulin-like growth factor receptor

Diabetes Mellitus Type 1

Ambiguity of the External Genitalia

Diabetes Mellitus Type 2

Fluids and electrolytes--clinical aspects

Chapter 154 - Disorders of the Adrenal Glands

Chapter 151 - Disorders of Pubertal Development

Chapter 152 - Disorders of Sexual Differentiation

Deletion of 3 basepairs resulting in the loss of lysine-121 in the insulin receptor alpha-subunit in a patient with leprechaunism: binding, phosphorylation, and biological activity

Melanocytic Nevi in Turner Syndrome

Growth hormone deficiency in an 8-year-old girl with human immunodeficiency virus infection

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

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