Давид Цанген

Научные публикации

• Characterization of 35 novel NR5A1/SF-1 variants identified in individuals with atypical sexual development: The SF1next study
• Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development
• Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development: a cross-sectional study
• Dasiglucagon for the Treatment of Congenital Hyperinsulinism: A Randomized Phase 3 Trial in Infants and Children
• Loss of function of FIGNL1, a DNA damage response gene, causes human ovarian dysgenesis
• Growth hormone therapy for children with Duchenne muscular dystrophy and glucocorticoid induced short stature
• ISPAD Clinical Practice Consensus Guidelines 2022: Ramadan and other religious fasting by young people with diabetes
• The utility of glucose area under the curve from the oral glucose tolerance test as a screening tool for cystic fibrosis-related diabetes
• Correction to: Early exposures and inherent factors in premature newborns are associated with type 1 diabetes
• Youth-onset type 2 diabetes in Israel: A national cohort
• Early exposures and inherent factors in premature newborns are associated with type 1 diabetes
• Nucleoporin107 mediates female sexual differentiation via Dsx
• Characterization of the Oral Microbiome Among Children With Type 1 Diabetes Compared With Healthy Children
• Eligibility for growth hormone therapy in children born small for gestational age is substantially lower than expected
• Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity
• NKX2-2 Mutation Causes Congenital Diabetes and Infantile Obesity With Paradoxical Glucose-Induced Ghrelin Secretion
• A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review
• The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD
• Birth during the moderate weather seasons is associated with early onset of type 1 diabetes in the Mediterranean area
• The novel R211Q POP1 homozygous mutation causes different pathogenesis and skeletal changes from those of previously reported POP1-associated anauxetic dysplasia
• Primary Ovarian Insufficiency Nationwide Incidence Rate and Etiology Among Israeli Adolescents
• Somatic growth in cystic fibrosis
• Adrenal function in cystic fibrosis
• Type 1 Diabetes Mellitus (Juvenile Diabetes) - A Review for the Pediatric Oral Health Provider
• Analysis of the genetic basis of height in large Jewish nuclear families
• Liraglutide in Children and Adolescents with Type 2 Diabetes
• BRCA2 in Ovarian Development and Function. Reply
• Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia
• Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy
• 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?
• Essential Role of BRCA2 in Ovarian Development and Function
• Prevalence of early and late prematurity is similar among pediatric type 1 diabetes patients and the general population
• Somapacitan, a once-weekly reversible albumin-binding GH derivative, in children with GH deficiency: A randomized dose-escalation trial
• GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome
• CFTR potentiator therapy ameliorates impaired insulin secretion in CF patients with a gating mutation
• A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis
• Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress
• Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure
• Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communication
• A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity
• Testicular differentiation factor SF-1 is required for human spleen development
• Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel
• Long duration of hyperglycemia in the first 96 hours of life is associated with severe intraventricular hemorrhage in preterm infants
• Euthyroid submedian free T4 and subclinical hypothyroidism may have a detrimental clinical effect in Down syndrome
• A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia
• Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War
• Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism
• XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription
• Expert opinion and clinical experience regarding patients with type 1 diabetes mellitus fasting on Yom Kippur
• Patients with cystic fibrosis and normoglycemia exhibit diabetic glucose tolerance during pulmonary exacerbation