1 Identification and Evaluation of Items for Vitreoretinal Diseases Quality of Life Item Banks.

2 A Neuropsychological Profile for Cerebrotendinous Xanthomatosis: A Single-Case Study.

3 Recommended Treatment for Antibody-mediated Rejection After Kidney Transplantation: the 2019 Expert Consensus From the Transplant Society Working Group.

4 TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

5 osler-weber-rendu syndrome: a case report with familial clustering

6 dubin-johnson syndrome. (a case report and review of literature).

7 from families syndromes to genes… the first clinical and genetic characterizations of hereditary syndromes predisposing to cancer: what was the beginning?

8 medical image of the week: bronchial clot removal via cryotherapy

9 Hereditary Diffuse Gastric Cancer: Prophylactic Surgical Oncology Implications

10 Genomic landscape of colorectal carcinogenesis.

11 The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.

12 Novel Deleterious nsSNPs within MEFV Gene that Could Be Used as Diagnostic Markers to Predict Hereditary Familial Mediterranean Fever: Using Bioinformatics Analysis

13 Identification and Mapping of a 2,009-bp DNA Deletion in SERPING1 of a Hereditary Angioedema Patient

14 Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn

15 Lactulose to the Rescue: A Case of Toxic Hepatic Encephalopathy Caused by Portosystemic Shunting and Epistaxis in a Patient with Hereditary Hemorrhagic Telangiectasia

16 A 40-Year-Old Male Presenting with Hereditary Multiple Exostosis: Management and Considerations

17 Multi gene panel testing for hereditary breast cancer - is it ready to be used?

18 Clinical application of whole exome sequencing in monogenic hereditary disorders in critically ill newborns

19 Cystic fibrosis transmembrane conductance regulator (CFTR) and autophagy: hereditary defects in cystic fibrosis gluten-mediated inhibition in celiac disease.

20 Characteristics and natural history of autonomic involvement in hereditary ATTR amyloidosis: a systematic review.

21 A Substantial Proportion of Apparently Heterozygous TP53 Pathogenic Variants Detected with a Next-Generation Sequencing Hereditary Pan-Cancer Panel Are Acquired Somatically.

22 Salvage procedures in lower-extremity trauma in a child with hereditary motor and sensory neuropathy type I: a case report

23 Genetics of hereditary hearing loss in east Iran population: A systematic review of mutations.

24 Food derived respiratory complex I inhibitors modify the effect of Leber hereditary optic neuropathy mutations.

25 Estimating the fiscal impact of rare diseases using a public economic framework: a case study applied to hereditary transthyretin-mediated (hATTR) amyloidosis.

26 A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).

27 Hereditary bilateral sudden sensorineural hearing loss.

28 Fresh frozen plasma for on-demand hereditary angioedema treatment in South Africa and Iran.

29 Disordered bone metabolism in hereditary spherocytosis patients.

30 Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

31 Hereditary acromegalic gigantism in the family of Roman Emperor Maximinus Thrax.

32 Identification of a comprehensive spectrum of genetic factors for hereditary breast cancer in a Chinese population by next-generation sequencing.

33 Cytodiagnosis and protein typing of amyloid from a vitreous washing: initial diagnostic workup of hereditary amyloidosis.

34 [Expert consensus on the management strategy of patients with hereditary ataxia during prevention and control of novel coronavirus pneumonia epidemic].

35 Clinical predictors of a positive test result in patients undergoing genetic evaluation for a hereditary kidney cancer syndrome.

36 Hereditary dentatorubral-pallidoluysian atrophy: ubiquitinated filamentous inclusions in the cerebellar dentate nucleus neurons

37 Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutation

38 [Hyperuricemia with cerebral paresis. Syndrome of a hereditary purine metabolic disorder]

39 [Hyperuricemia with cerebral paresis. Syndrome of a hereditary purine metabolic disorder].

40 Heparan sulfate proteoglycan expression in cerebrovascular amyloid β deposits in Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis (Dutch) brains

41 Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I

42 Degeneration of anterior horn cell in neuronal type of Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type II): A Golgi study

43 white spongy nevus: a nonhereditary presentation

44 molecular diagnosis of hereditary nonpolyposis colorectal cancer (lynch syndrome)

45 analysis of genetic mutations in a cohort of hereditary optic neuropathy in shanghai, china

46 existence of solutions to a self-referred and hereditary system of differential equations

47 management of hereditary breast cancer

48 hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3

49 alterações moleculares associadas à hemocromatose hereditária molecular changes associated with hereditary hemochromatosis

50 the usage of integral equations hereditary theories for calculating changes of measures of the theory of damage when exposed to repeated loads

51 hereditary apolipoprotein ai-associated renal amyloidosis: a diagnostic challenge

52 hereditary angioedema: the economics of treatment of an orphan disease

53 multispeciality approach in the management of patient with hereditary gingival fibromatosis: 1-year followup: a case report

54 hereditary fibrinogen aα-chain amyloidosis in asia: clinical and molecular characteristics

55 woman presenting with chronic iron deficiency anemia associated with hereditary hemorrhagic telangiectasia: a case report

56 the hereditary spectrum of pancreatic cancer: the edmonton experience

57 isquemia segmentaria de yeyuno como complicación de trombosis venosa mesentérica secundaria a déficit congénito de antitrombina iii segmentary yeyunal ischemia complicating mesenteric vein thrombosis secondary to a hereditary antithrombin deficit

58 spinal cord infarction in a patient with hereditary spherocytosis: a case report and discussion

59 new forms of -compactness with respect to hereditary classes

60 copy number variation in hereditary non-polyposis colorectal cancer

61 rivaroxaban treatment for warfarin-refractory thrombosis in a patient with hereditary protein s deficiency

62 hereditary angioedema by c1 inhibitor-deficit: diagnostic and therapeutic challenges. case report

63 orthodeoxia without platypnea in hereditary hemorrhagic telangiectasia in the presence of a cerebral abscess and multiple pulmonary arteriovenous malformations: unusual complications and transcatheter endovascular treatment

64 the domestic cat as a large animal model for characterization of disease and therapeutic intervention in hereditary retinal blindness

65 cognitive impairment involving social cognition in spg4 hereditary spastic paraplegia

66 metastasis of pregnancy-associated breast cancer (suspected to be hereditary breast and ovarian cancer) to the brain, diagnosed at 18 weeks’ gestation: a case report and review of the literature

67 heat shock response associated with hepatocarcinogenesis in a murine model of hereditary tyrosinemia type i

68 on the order hereditary closure preserving sum theorem

69 hereditary angioedema and gastrointestinal complications: an extensive review of the literature

70 orphan hereditary syndromes in the practice of pediatric endocrinologist

71 anti-angiogenic therapeutic strategies in hereditary hemorrhagic telangiectasia

72 clinical and neurophysiologic characterization of an european family with hereditary sensory neuropathy, paroxysmal cough and gastroesophageal reflux

73 note on generalized topological spaces with hereditary classes

74 generation of induced pluripotent stem cells (ipscs) from a hereditary spastic paraplegia patient carrying a homozygous y275x mutation in cyp7b1 (spg5)

75 multiplex partial nephrectomy, repeat partial nephrectomy, and salvage partial nephrectomy remain the primary treatment in multifocal and hereditary kidney cancer

76 circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia

77 hereditary angioedema presenting as irritable bowel syndrome: a case of early closure

78 hereditary neuropathy with liability to pressure palsy: a recurrent and bilateral foot drop case report

79 management of acute attacks of hereditary angioedema: role of ecallantide

80 hereditary leiomyomatosis with renal cell carcinoma

81 Investigation of apc, mlh1 and msh2 mutations in patients with hereditary colorectal carcinoma: A single center experience

82 The genetics and natural history of hereditary colon cancer.

83 Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage

84 Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia

85 Mutation of an mutL Homologue in a Navajo Family With Hereditary Nonpolyposis Colorectal Cancer

86 Mismatch Repair Genes on Chromosomes 2p and 3p Account for a Major Share of Hereditary Nonpolyposis Colorectal Cancer Families Evaluable by Linkage

87 Genotypic and Phenotypic Characteristics of Hereditary Colorectal Cancer.

88 Prevalence of Hereditary Diseases of the Nervous System in Uzbekistan on the Example of the City of Tashkent

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