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Here Comes the Sun: Medical Professionalism and the Implications of the Sunshine Act for Gastroenterology Practice
Here comes the sun: multimodal displays are associated with sunlight incidence
Hereditary haemorrhagic telangiectasia, an Australian cohort: clinical and investigative features
Hereditarily supercompact spaces
Hereditary multiple exostoses: anatomical distribution and burden of exostoses is dependent upon genotype and gender
Hereditary gynecological tumors associated with Peutz-Jeghers syndrome
Hereditary gene mutations in Korean patients with isolated erythrocytosis
Hereditary Leiomyomatosis and Renal Cell Carcinoma (HLRCC) A Rapid Autopsy Report of Metastatic Renal Cell Carcinoma
Hereditary breast and ovarian cancer and reproduction: an observational study on the suitability of preimplantation genetic diagnosis for both asymptomatic carriers and breast cancer survivors
Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain
Hereditary vulnerabilities to post-operative cognitive dysfunction and dementia
Hereditary Hemochromatosis: Missed Diagnosis or Misdiagnosis?
Hereditary thrombophilia in cerebral venous thrombosis: a study from India
Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking
Hereditary Breast/Ovarian Cancer Syndrome A Primer for Obstetricians/Gynecologists
Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12
Here We Go Again Reply
Hereditary breast and ovarian cancer: lessening the burden
Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms
Hereditary Spastic Paraplegia: Clinical Principles and Genetic Advances
Hereditary Kidney Cancer Syndromes
Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position
Here today, here tomorrow: Beached timber in Gabon, a persistent threat to nesting sea turtles
Hereditary gynecologic cancers
Hereditary ovarian and breast cancer: what have we learned?
Hereditary unigraphs and Erdos-Gallai equalities
Hereditary angioedema: a brief review of new developments
Here Come the Sleep Apnea-Cancer Studies
Here be dragons: a tool for quantifying novelty due to covariate range and correlation change when projecting species distribution models
Here come the newcomer granules, better late than never
Hereditary ataxias: overview
Hereditary Angioedema as the Cause of Death from Asphyxia: Postmortem Computed Tomography Study
Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany
Hereditary myopathy with early respiratory failure: occurrence in various populations
Hereditary elliptocytosis
Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome
Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes
Here and now and the New Year 2014
Heredity, development and evolution: the unmodern synthesis of ES Russell
Hereditary Ataxia and Spastic Paraplegia in Portugal A Population-Based Prevalence Study
Hereditary nephrogenic diabetes insipidus in Japanese patients: analysis of 78 families and report of 22 new mutations in AVPR2 and AQP2
Hereditary disorders affecting the lacrimal system
Hereditary transthyretin amyloidosis
Hereditary Medullary Thyroid Cancer: Age-Appropriate Thyroidectomy Improves Disease-Free Survival
Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry
Hereditary angioedema: a bradykinin-mediated swelling disorder
Hereditary gynaecological malignancies: advances in screening and treatment
Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2
Hereditary prostate cancer
Hereditary angioedema due to C1 inhibitor deficiency
Here Come the Exchange Patients
Hereditary diffuse leukencephalopathy with spheroids. A microgliopathy due to CSF1 receptor impairment
Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1
Hereditary myopathy with early respiratory failure is associated with misfolding of the titin fibronectin III 119 subdomain
Hereditary erythrocytosis, thrombocytosis and neutrophilia
Hereditary lissencephaly and cerebellar hypoplasia in Churra lambs
Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation
Hereditary Spherocytosis and Wandering Spleen