congenital - Globe Thesis

Keyword [congenital] Result: 1 - 20 \| Page: 1 of 10
1.	The Status Of Immunological And Parathroid Function In Children With Congenital Heart Disease
2.	The Clinical Aspects And Molecule Mechanisms Of Congenital Coagulation Factor V Deficiency: Studies Of Two Families
3.	Evaluation Of The Anal Sphincter Function Qualitatively And Quantitatively With Vector Manometry In Clinical Patients And Experimental Dogs
4.	Study On The Growth Of Endothelial Cells To Polyamide, A Novel Material For The Catheter Occlusion Of Congenital Heart Disease, And Clinical Evaluation Of The Transcatheter Occlusion Of Congenital Heart Disease
5.	The Evaluation Of Right Ventricular Function In Patient With Atrial Septal Defect And To Research The Pathogenesis Of Secondary Pulmonary Hypertension In Patient With Congenital Heart Disease
6.	The Study Of Therapeutic Mechanism Of Glucocorticoid By Injection Into Sternocleidomastoid Muscle In CMT
7.	Location And Identification Of Human Simple Congenital Heart Disease Susceptibility Genes
8.	The Genetic Studies On Causative Gene For Congenital Hypoplasia Of Teeth Root
9.	Effect Of Shanjikeli On Congenital CMV Infection Inhibition
10.	Molecular Genetics Of Pathogenesis Of Congenital Nephrogenic Diabetes Insipidus
11.	Mapping The Locus For Congenital Preauricular Fistula And A Study Of The Candidate Gene To Schizophrenia
12.	Localization And Cloning The Disease-associated Gene Of A Special Fasciculiform Congenital Cataract
13.	The Effects Of Nonpulsatile Flow After Fontan Operation On Pulmonary Microvascular Circulation
14.	Congenital Dislocation Of The Hip: Study Of Genetic Epidemiology And Associations With HOXB9 And COL1A1 Genes
15.	Studies Of Adhesion Molecules Expression In Children With Congenital Hydronephrosis And Evaluation Of Renal Function By Nuclide Nephro-Dynamic Imaging
16.	Study On The Effect Of Adrenomedullin, Urotensin-Ⅱ And Nitric Oxide On Pulmonary Hypertension Of Patients With Congenital Heart Disease
17.	Congenital Fibrosis Of The Extraocular Muscles In Chinese Families: Clinical Phenotype, Linkage Mapping, And Mutation Identification Of KIF21A
18.	Study Of Candidate Genes In Congenital Inherited Nuclear Cataract
19.	The Study On Mutation In Congenital Hypothyroidism
20.	Experiments In Pathogenesis And Treatment Of Lung Hypoplasia With Congenital Diaphragmatic Hernia
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