Hypophosphatemic - Globe Thesis

Keyword [Hypophosphatemic] Result: 1 - 19 \| Page: 1 of 1
1.	Genetic Studies Of Low-phosphorus Rickets / Osteomalacia Dysplasia Of Bone Resistance Of Fibrous Tissue Gene Mutation Detection
2.	Genetic Analysis Of Patients With Hypophosphatemic Rickets
3.	Part Ⅰ:Clinical Spectrum Of X-Linked Hypophosphatemia In Adults Part Ⅱ:Genetic Fusion Of Phosphaturic MesenchymalTumors
4.	Research On Clinical And Molecular Etiology Of Monogenic Hereditary Bone Disease
5.	Clinical Features, Early Diagnosis And Early Treatment Of Hypophosphatemic Osteomalacia Due To Fanconi’s Syndrome Secondary To Adefovir Dipivoxil
6.	Constructing LCA-Nmnat1 Mice Models Using CRISPR-Cas9 Technology And Its Pathogenesis Research And A De Novo Mosaic Mutation Of PHEX Gene Causing Hypophosphatemic Rickets
7.	Effects Of Hypophosphatemia On The Ability Of Daily Life Of In-patients With Advanced Age
8.	Study Of The Molecular Mechanism In Two X-linked Hypophosphatemic Rickets Pedigrees
9.	Clinical Analysis Of 10 Cases Of Hypophosphatemic Osteomalacia And Literature Review
10.	Adefovir Depivoxil Induced Hypophosphatemic Osteomalacia In Chronic Hepatitis B:a Comparative Study From Chinese And Foreign Case Series
11.	Targeted Gene Sequencing For Hypophosphatemic Rickets And Osteomalacia
12.	1. The Clinical And Molecular Genetic Study Of X-linked Dominant Hypophosphatemia Rickets 2. A Prospective, Open, Follow-up Study Of High/low Dose Active Vitamin D Combined With Neutral Phosphorus In The Treatment Of Children With XLH
13.	The Construction Of DMP1 Knockout Rabbit Model Of Hypophosphatemic Rickets
14.	Analysis The Clinical Characteristics Of Hypophosphatemic Osteomalacia Due To Adefovir Dipivoxil
15.	Study On The Clinical And Genetic Characteristics Of Rickets Related To Hereditary Renal Tubular Disease
16.	Study On The Pathogenic Mutations Of Two Single-gene Inherited Diseases Of The Locomotion System
17.	Clinical And Molecular Genetic Mechanism Of FGF23 Mutation-related Diseases. Study On The Metabolic Regulation Mechanism Of ENPP1 On FGF23
18.	Molecular Genetics Of X-linked Hypophosphatemic Rickets In Children
19.	Molecular Diagnosis Of Hypophosphatemic Rickets And Functional Research Of Novel Mutations In PHEX Gene In Vitro
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