Yalei Pi

Clinical and molecular spectrum of patients with methylmalonic acidemia and homocysteinemia complicated by cardiovascular manifestations

Orphanet Journal of Rare Diseases 2025cited by 1position: middledoi

[Zhu-Tokita-Takenouchi-Kim syndrome in a neonate].

PubMed 2025cited by 0position: middledoi

Growth characteristics of children with 21-hydroxylase deficiency and the value of steroid hormones in height assessment

BMC Pediatrics 2025cited by 0position: middledoi

Comprehensive characterization of 21-hydroxylase deficiency in a Chinese pediatric cohort: phenotype, steroid profiles and genetics

Frontiers in Endocrinology 2025cited by 0position: middledoi

Impact of All-trans Retinoic Acid on Skeletal Development: Mechanisms of Growth Plate Closure

Combinatorial Chemistry & High Throughput Screening 2025cited by 0position: middledoi

Longitudinal skeletal growth and growth plate morphological characteristics of chondro-tissue specific CUL7 knockout mice

Annals of Anatomy - Anatomischer Anzeiger 2024cited by 1position: middledoi

Inhibition of LAMP3 mediates the protective effect of vitamin D against hypoxia/reoxygenation in trophoblast cells

Brazilian Journal of Medical and Biological Research 2023cited by 4position: lastdoi

ERα/β/DMP1 axis promotes trans‐differentiation of chondrocytes to bone cells through GSK‐3β/β‐catenin pathway

Journal of Anatomy 2022cited by 17position: middledoi

Vitamin D alleviates hypoxia/reoxygenation-induced injury of human trophoblast HTR-8 cells by activating autophagy

Placenta 2021cited by 18position: firstdoi

[Nephrogenic syndrome of inappropriate antidiuresis manifested by recurrent hyponatremia and convulsions].

PubMed 2021cited by 0position: middledoi

A diagnostic model of idiopathic central precocious puberty based on transrectal pelvic ultrasound and basal gonadotropin levels

Journal of International Medical Research 2020cited by 17position: middledoi

[Acute pancreatitis as an initial manifestation of parathyroid adenoma].

PubMed 2020cited by 0position: middledoi

Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome

Orphanet Journal of Rare Diseases 2019cited by 20position: middledoi

Methylmalonic Acidemia Complicated by Homocystinuria Diseases: a Report of Three Cases

Advances in Therapy 2019cited by 5position: middledoi

[Clinical and mutational analysis of 7 children with X-linked adrenal dysplasia congenita].

PubMed 2019cited by 0position: firstdoi

Comparative study of GnRHa stimulation test and GnRH stimulation test

International journal of pediatrics 2019cited by 0position: middledoi

[Clinical features and genetic analysis of seven patients with congenital hyperinsulinism].

PubMed 2018cited by 2position: middledoi

A novel mutation causes autosomal recessive pseudohypoaldosteronism type I

Zhonghua shiyong erke linchuang zazhi 2018cited by 0position: firstdoi

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