Detalhe da pesquisa
1.
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy.
Hum Mol Genet
; 29(11): 1772-1783, 2020 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31108500
2.
Alarming increase in ketoacidosis in children and adolescents with newly diagnosed type 1 diabetes during the first wave of the COVID-19 pandemic in Israel.
Pediatr Diabetes
; 23(1): 10-18, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34865288
3.
A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly.
Am J Med Genet A
; 185(10): 3161-3166, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34145742
4.
Environmental rather than genetic factors determine the variation in the age of the infancy to childhood transition: a twins study.
J Pediatr
; 166(3): 731-5, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25578994
5.
Predicting pubertal development by infantile and childhood height, BMI, and adiposity rebound.
Pediatr Res
; 78(4): 445-50, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26151490
6.
Energy Trade-off and 4 Extreme Human Body Types.
J Clin Endocrinol Metab
; 108(5): e89-e97, 2023 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36413496
7.
Family Size and the Age at Infancy-Childhood Transition Determine a Child's Compromised Growth in Large Families.
Front Pediatr
; 10: 821048, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35573956
8.
Periorbital inflammation associated with craniofacial fibrous dysplasia: Report of three cases and review of the literature.
Bone
; 153: 116157, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34425287
9.
Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism.
Thyroid
; 31(2): 202-207, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32718224
10.
Prediction of Adult Height by Machine Learning Technique.
J Clin Endocrinol Metab
; 106(7): e2700-e2710, 2021 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33606028
11.
Sexual Dimorphism of Size Ontogeny and Life History.
Front Pediatr
; 8: 387, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32793524
12.
People Are Taller in Countries With Better Environmental Conditions.
Front Endocrinol (Lausanne)
; 11: 106, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32218770
13.
Primary Ovarian Insufficiency Nationwide Incidence Rate and Etiology Among Israeli Adolescents.
J Adolesc Health
; 66(5): 603-609, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31987720
14.
Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia.
J Clin Endocrinol Metab
; 104(8): 3172-3180, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30865229
15.
Control of childhood congenital adrenal hyperplasia and sleep activity and quality with morning or evening glucocorticoid therapy.
J Clin Endocrinol Metab
; 93(12): 4707-10, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18782876
16.
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal.
Horm Res Paediatr
; 88(2): 127-139, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28689203
17.
Validation of a Novel Assay to Distinguish Bacterial and Viral Infections.
Pediatrics
; 140(4)2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28904072
18.
Consecutive mutational events in a TSHR allele of Arab families with resistance to thyroid stimulating hormone.
Thyroid
; 22(3): 252-7, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22313426
19.
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
Clin Endocrinol (Oxf)
; 66(5): 695-702, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17381485