D. Zangen

发表

Vulnerability of Islets in the Immediate Posttransplantation Period: Dynamic Changes in Structure and Function

S. Bonner-Weir, G. Weir, A. Davalli, 1996, Diabetes.

Patients with cystic fibrosis and normoglycemia exhibit diabetic glucose tolerance during pulmonary exacerbation.

E. Kerem, D. Zangen, D. Shoseyov, 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Somatic growth in cystic fibrosis.

D. Zangen, E. Lavi, Alex Gileles-Hillel, 2019, Current opinion in endocrinology, diabetes, and obesity.

Establishing glycaemic control with continuous subcutaneous insulin infusion in children and adolescents with type 1 diabetes: experience of the PedPump Study in 17 countries

P. Hindmarsh, M. Phillip, O. Kordonouri, 2008, Diabetologia.

Exercise stimulates the mitogen-activated protein kinase pathway in human skeletal muscle.

R. Fielding, S. Dufresne, D. Aronson, 1997, The Journal of clinical investigation.

CFTR potentiator therapy ameliorates impaired insulin secretion in CF patients with a gating mutation.

E. Kerem, D. Zangen, G. Livnat, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Early exposures and inherent factors in premature newborns are associated with type 1 diabetes

O. Eyal, I. Morag, M. Rachmiel, 2022, Pediatric Research.

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

S. Shalitin, M. Rachmiel, O. Pinhas-Hamiel, 2012, Pediatric diabetes.

Pancreatic Duodenal Homeobox (PDX-1) in Health and Disease

A. Tsur, D. Zangen, D. Melloul, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Impaired Glucose-Stimulated Insulin Secretion Is Coupled With Exocrine Pancreatic Lesions in the Cohen Diabetic Rat

N. Kaiser, S. Lenzen, I. Raz, 2008, Diabetes.

Birth during the moderate weather seasons is associated with early onset of type 1 diabetes in the Mediterranean area

S. Shalitin, O. Eyal, M. Rachmiel, 2020 .

Prevalence of early and late prematurity is similar among pediatric type 1 diabetes patients and the general population

S. Shalitin, O. Eyal, M. Rachmiel, 2018, Diabetes/metabolism research and reviews.

The newly inbred cohen diabetic rat: a nonobese normolipidemic genetic model of diet-induced type 2 diabetes expressing sex differences.

H. Jacob, A. Ornoy, D. Zangen, 2001, Diabetes.

Youth‐onset type 2 diabetes in Israel: A national cohort

M. Phillip, M. Rachmiel, K. Mazor Aronovitch, 2022, Pediatric diabetes.

Extracellular-regulated protein kinase cascades are activated in response to injury in human skeletal muscle.

O. Ljungqvist, R. Fielding, D. Aronson, 1998, American Journal of Physiology - Cell Physiology.

Early changes in syngeneic islet grafts: effect of recipient's metabolic control on graft outcome.

S. Bonner-Weir, G. Weir, A. Davalli, 1995, Transplantation proceedings.

A Novel Familial Mutation in the PCSK1 Gene That Alters the Oxyanion Hole Residue of Proprotein Convertase 1/3 and Impairs Its Enzymatic Activity

I. Lindberg, O. Pappo, Martín G. Martín, 2014, PloS one.

Extracellular-regulated protein kinase cascades are activated in response to injury in human skeletal muscle.

O. Ljungqvist, R. Fielding, D. Aronson, 1998, American journal of physiology. Cell physiology.

Adrenal function in cystic fibrosis.

D. Zangen, A. Kelly, K. Hughan, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.

E. Levy-Lahad, D. Zangen, P. Renbaum, 2012, European journal of endocrinology.

GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome.

R. Mittler, R. Nechushtai, O. Pappo, 2016, The Journal of clinical endocrinology and metabolism.

Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity

R. Zarivach, A. Haim, D. Zangen, 2021, American journal of medical genetics. Part A.

Bilateral Medullary Thyroid Carcinoma in a 3-Year-Old Female Patient with Multiple Endocrine Neoplasia 2A Syndrome Undergoing Prophylactic Thyroidectomy: Should Current Guidelines Be Revised?

S. Grozinsky-Glasberg, D. Zangen, H. Mazeh, 2018, European Thyroid Journal.

Accurate prediction of children's target height from their mid-parental height

L. Kruglyak, D. Zangen, D. Zeevi, 2022, medRxiv.

Novel de novo mutation in SUR1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence

B. Glaser, D. Zangen, Maha Abdulhadi-Atwan, 2008 .

Transcription factor abnormalities as a cause of beta cell dysfunction in diabetes: a hypothesis

S. Bonner-Weir, G. Weir, A. Sharma, 1997, Acta Diabetologica.

The Role of Reactive Oxygen Species in Diabetes-Induced Anomalies in Embryos of Cohen Diabetic Rats

A. Ornoy, D. Zangen, S. Shechtman, 2002, International journal of experimental diabetes research.

The homeodomain protein IDX-1 increases after an early burst of proliferation during pancreatic regeneration.

S. Bonner-Weir, G. Weir, A. Sharma, 1999, Diabetes.

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure

D. Bercovich, Dvir Dahary, S. Gulsuner, 2015, Journal of Medical Genetics.

Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy.

P. White, M. Korner, D. Zangen, 2010, European journal of endocrinology.

Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy

Gheona Altarescu, Aharon Peretz, Shai Carmi, 2018, Genetics in Medicine.

Role of a founder c.201_202delCT mutation and new phenotypic features of congenital lipoid adrenal hyperplasia in Palestinians.

W. Chung, I. Lerer, S. Ten, 2007, The Journal of clinical endocrinology and metabolism.

Prenatal diagnosis of congenital lipoid adrenal hyperplasia (CLAH) by estriol amniotic fluid analysis and molecular genetic testing

W. Chung, M. Mansukhani, I. Lerer, 2008, Prenatal diagnosis.

The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD

D. Behar, R. Segel, E. Levy-Lahad, 2020, Endocrine.

XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.

Ayal B. Gussow, L. Carmel, E. Levy-Lahad, 2011, American journal of human genetics.

A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis.

E. Levy-Lahad, D. Zangen, A. Samson, 2015, The Journal of clinical investigation.

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

L. Carmel, E. Levy-Lahad, D. Zangen, 2015, Journal of Medical Genetics.

Characterization of the Oral Microbiome Among Children With Type 1 Diabetes Compared With Healthy Children

M. Yassour, D. Steinberg, D. Zangen, 2021, Frontiers in Microbiology.

Long duration of hyperglycemia in the first 96 hours of life is associated with severe intraventricular hemorrhage in preterm infants.

D. Zangen, B. Bar‐Oz, T. Bdolah-Abram, 2013, The Journal of pediatrics.

Testicular differentiation factor SF-1 is required for human spleen development.

C. Flück, N. Camats, E. Levy-Lahad, 2014, The Journal of clinical investigation.

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence

B. Glaser, S. Shyng, D. Zangen, 2008, Diabetes.

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.

A. Eliakim, B. Glaser, L. Aguilar-Bryan, 2004, The Journal of clinical endocrinology and metabolism.

Primary Ovarian Insufficiency Nationwide Incidence Rate and Etiology Among Israeli Adolescents.

A. Eliakim, Y. Shoenfeld, O. Eyal, 2020, The Journal of adolescent health : official publication of the Society for Adolescent Medicine.

Nucleoporin107 mediates female sexual differentiation via Dsx

G. Deshpande, D. Zangen, O. Gerlitz, 2021, bioRxiv.

Euthyroid Submedian Free T4 and Subclinical Hypothyroidism May Have a Detrimental Clinical Effect in Down Syndrome

D. Zangen, A. Tenenbaum, E. Lebel, 2012, Hormone Research in Paediatrics.

Serum lidocaine concentrations in children during bronchoscopy with topical anesthesia.

N. Noviski, A. Avital, Y. Amitai, 1990, Chest.

NKX2-2 mutation causes congenital diabetes and infantile obesity with paradoxical glucose induced ghrelin secretion.

M. King, R. Hemi, S. Gulsuner, 2020, The Journal of clinical endocrinology and metabolism.

Analysis of the genetic basis of height in large Jewish nuclear families

L. Kruglyak, J. Bloom, E. Levy-Lahad, 2018, bioRxiv.

Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia.

S. Almashanu, A. Eliakim, B. Pode-Shakked, 2019, The Journal of clinical endocrinology and metabolism.

Relative Expression of a Dominant Mutated ABCC8 Allele Determines the Clinical Manifestation of Congenital Hyperinsulinism

B. Glaser, S. Shyng, R. Shemer, 2011, Diabetes.

ISPAD Clinical Practice Consensus Guidelines 2022: Ramadan and other religious fasting by young people with diabetes

M. Marcovecchio, A. Deeb, D. Zangen, 2022, Pediatric diabetes.

Type 1 diabetes and prolonged fasting

D. Zangen, N. Shehadeh, A. Tzur, 2007, Diabetic medicine : a journal of the British Diabetic Association.

Arginine and Clonidine Stimulation Tests for Growth Hormone Deficiency Revisited - Do We Really Need So Many Samples?

D. Zangen, R. Nesher, H. Hirsch, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Expert opinion and clinical experience regarding patients with type 1 diabetes mellitus fasting on Yom Kippur

D. Zangen, M. Grajower, 2011, Pediatric diabetes.

[Diabetic patients in the Yom Kippur fast--who can fast and how to treat the fasting patients].

G. Leibowitz, D. Zangen, Y. Katz, 2009, Harefuah.

The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.

B. Glaser, O. Elpeleg, V. Doviner, 2008, Journal of the American Academy of Dermatology.

Essential Role of BRCA2 in Ovarian Development and Function

Matt A. King, M. Goldberg, S. Gulsuner, 2018, The New England journal of medicine.

Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communication

H. Huopio, C. Stanley, M. Polak, 2015, Diabetic medicine : a journal of the British Diabetic Association.

Reduced Insulin, GLUT2, and IDX-1 in β-Cells After Partial Pancreatectomy

S. Bonner-Weir, G. Weir, J. Habener, 1997, Diabetes.

The novel R211Q POP1 homozygous mutation causes different pathogenesis and skeletal changes from those of previously reported POP1‐associated anauxetic dysplasia

E. Levy-Lahad, D. Zangen, P. Renbaum, 2020, American journal of medical genetics. Part A.

Indomethacin and apnea of prematurity.

C. Hammerman, D. Zangen, 1993, Critical care medicine.

Impaired glucose metabolism in patients with CF during acute exacerbations

E. Kerem, D. Zangen, D. Shoseyov, 2008 .

Eligibility for growth hormone therapy in children born small for gestational age is substantially lower than expected

D. Zangen, C. Stein-Zamir, H. Shoob, 2021, Clinical endocrinology.

The utility of glucose area under the curve from the oral glucose tolerance test as a screening tool for cystic fibrosis‐related diabetes

E. Kerem, D. Zangen, A. Sprikkelman, 2022, Pediatric Pulmonology.

Mutations in DDR2 gene cause SMED with short limbs and abnormal calcifications.

J. Melki, J. Sosna, R. Belostotsky, 2009, American journal of human genetics.

L. Carmel, E. Levy-Lahad, D. Zangen, 2015, Journal of Medical Genetics.

Growth hormone therapy for children with Duchenne muscular dystrophy and glucocorticoid induced short stature.

T. Dor, D. Zangen, R. Tsabari, 2023, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.