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Hereditary optic neuropathies
Hereditary and Sporadic Cerebral Microvascular Diseases Introduction
Hereditary prostate cancer as a feature of Lynch Syndrome
Hereditary angioedema (HAE) in children and adolescents. Consensus on therapeutic strategies
Hereditary angioedema (HAE) in children and adolescents-a consensus on therapeutic strategies
Hereditary cardiac amyloidosis with transthyretin mutations. A cause of sudden death
Hereditary gingival hyperplasia associated with amelogenesis imperfecta: A case report
Hereditary Systemic Amyloidosis Due to Asp76Asn Variant beta(2)-Microglobulin
Hereditary hemorrhagic telangiectasia: An overview of diagnosis, management, and pathogenesis
Hereditary Angioedema Therapies in the United States: Movement Toward an International Treatment Consensus
Here it comes .... the role of cost-effective analysis
Hereditary Angioedema in Japan: Genetic Analysis of 13 Unrelated Cases
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family
Heredity Produced: At the Crossroads of Biology, Politics and Culture 1500-1870.
Hereditary approximation property
Hereditary eye dieseas in the Entlebucher Mountaindog in Switzerland: A retrospective study from 1999 to 2009
Hereditary angioedema: Historical aspects, classification, pathophysiology, clinical presentation, and laboratory diagnosis
Heredity diversity in populations of free-, self-, and specific cross-pollinated progenies of some olive (Olea europaea L.) cultivars
Heregulin beta-1 Induces Loss of Cell-Cell Contact and Enhances Expression of MUC1 at the Cell Surface in HCC2998 and MKN45-1 Cells
Hereditary thrombophilia in an unselected cohort of venous thrombosis patients in Singapore
Heredity between the Middle Ages and Modern Times: Historical Perspectives
Heredity of bicuspid aortic valve: is family screening indicated?
Hereditary isolated metatarsophalangeal arthritis
Hereditary angioedema: A case of near fatal laryngeal swelling in a 41-year-old woman
Hereditary breast cancer: clinical features and risk reduction strategies
Hereditary Hypophosphatemic Rickets With Hypercalciuria and Nephrolithiasis-Identification of a Novel SLC34A3/NaPi-IIc Mutation
Hereditary angioedema: Classification, pathogenesis, and diagnosis
Hereditary Vitamin D-Resistant Rickets (HVDRR) Owing to a Heterozygous Mutation in the Vitamin D Receptor
Hereditary Phosphofructokinase Deficiency in Wachtelhunds
Hereditary quasirandom properties of hypergraphs
Hereditary angioedema: A clinical review for the otolaryngologist
Hereditary structure in Hamiltonians: Information geometry of Ising spin chains
Heredity in epilepsy - An historical overview
Hereditary angioedema: Management of laryngeal attacks
Hereditary Cancer Syndromes: If You Look, You Will Find Them
Hereditary angioedema: Short-term prophylaxis for surgery
Here We Are! Where Are We? Locating Mixed Reality in The Age of the Smartphone
Here to stay: Clinician investigator training in a changing environment
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial
Hereditary Renal Cystic Disorders: Imaging of the Kidneys and Beyond
Hereditary Hypotrichosis Simplex of the Scalp
Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu syndrome)
Hereditary Angioedema: Implications of Management
Here come the commensals
Heregulin-1 beta and HER3 in hepatocellular carcinoma: status and regulation by insulin (vol 35, 126, 2016)
Heregulin-1 beta and HER3 in hepatocellular carcinoma: status and regulation by insulin
Hereditary leiomyomatosis and renal cell cancer syndrome: An update and review
Hereditary spastic paraplegia: More than an upper motor neuron disease
Hereditary Predispositions to Myelodysplastic Syndrome
Hereditary Orotic Aciduria and the Excretion of Orotidine
Hereditary persistence of alpha-fetoprotein
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
Hereditary Hyperferritinemia Cataract Syndrome: Clinical, Genetic, and Laboratory Findings in 5 Families
Hereditary episodic ataxia
Hereditarily indecomposable Banach algebras of diagonal operators
Hereditary Spherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II
Hereditary isolated ossicular anomalies in two generations of patients
Here We Go Again