Neurofibromatosis-Noonan syndrome and growth deficiency in an Iranian girl due to a pathogenic variant in NF1 gene.

Autor: Dalili, Setila, Hoseini Nouri, Seyyedeh Azade, Bayat, Reza, Koohmanaee, Shahin, Tabrizi, Manijeh, Zarkesh, Marjaneh, Tarang, Alireza, Mahdieh, Nejat

Publikováno v: Human Genomics; 2/20/2023, Vol. 17 Issue 1, p1-6, 6p

The Association Between Hemoglobin HbA1c with Serum Inorganic Phosphate in Children with Type 1 Diabetes.

Autor: Dalili S; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran., Koohmanaee S; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran., Nemati SAR; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran., Hoseini Nouri SA; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran., Hassanzadeh Rad A; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran., Kooti W; Lung Diseases & Allergy Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.

Publikováno v: Diabetes, metabolic syndrome and obesity : targets and therapy [Diabetes Metab Syndr Obes] 2020 Sep 29; Vol. 13, pp. 3405-3409. Date of Electronic Publication: 2020 Sep 29 (Print Publication: 2020).