GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).
about
Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmiasPrediction of gene-phenotype associations in humans, mice, and plants using phenologsZebrafish model for human long QT syndromeInherited diseases of the inner ear in man in the light of studies on the mousePROFOUND CHILDHOOD DEAFNESS.Surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval present at birth, and severe anaemia and syncopal attacks in childhoodLeft stellate ganglionectomy for the long Q-T interval syndrome: nine-year follow-up of a patient.Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.Jervell and Lange-Nielsen syndrome in a father and daughter from a large highly inbred family: a 16-year follow-up of 59 living members.Hereditary prolongation of QT interval . Study of two families.Hereditary prolongation of QT intervalAtrioventricular dissociation with prolonged QT interval and syncopal attacks in a 10-year-old boy.Cardio-auditory syndromes. Cardiac and genetic study of 511 deaf-mute childrenSurdo-cardiac syndrome: incidence among children in schools for the deaf.A study of the inheritance pattern of Romano-Ward syndrome. Prolonged Q-T interval, syncope, and sudden death.A case of the cardio-auditory syndrome (long QT interval and profound deafness) diagnosed in the perinatal period and kept under surveillance for two years.Consanguinity, cardiac arrest, hearing impairment, and ECG abnormalities: counselling pitfalls in the Romano-Ward syndrome.Drug-induced QT interval shortening: potential harbinger of proarrhythmia and regulatory perspectives.Novel Kv7.1-phosphatidylinositol 4,5-bisphosphate interaction sites uncovered by charge neutralization scanningMutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.Sudden unexpected death in infants ("cot death"). Report of a collaborative study in northern Ireland.Sudden unexpected death in infants. Evidence on a lethal cardiac arrhythmia.Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosityGenotype- and phenotype-guided management of congenital long QT syndrome.Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome.Case 1: An infant with a low heart rate.Hereditary congenital severe deafness syndromes.Rheumatic fever: a ten year review of patients admitted to an Irish children's hospital. Diagnosis.A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.Genetics, molecular mechanisms and management of long QT syndrome.DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
P2860
Q24314905-38AC77E4-A668-4DD5-968D-3360AD6B1503Q28679989-4BD3376E-0797-4806-8C29-F076948D5EE6Q30480271-546E2976-4C5E-412E-B3FB-2069B0EC10B7Q30495431-253D2B75-5BB5-49DC-AADE-22FF3F1467EAQ30495432-D3612761-2498-4708-BB5D-247D6F19E8BCQ33147524-45CFEBBC-D936-4163-B29D-F9D0B0173953Q33151539-EEC9F43F-DE67-441F-866B-7882600D90F4Q33153847-15543636-DA1A-4913-8A76-E9A768C10405Q33162763-B9CC146C-EC63-4EF5-8FE1-F8862F558A7DQ33170558-7DF499C2-A89C-4A99-90D8-E08EF35E81DAQ33170564-7B221428-0F93-4B98-96BA-E4D7D1B5ED6EQ33171053-3A970C6A-0B37-4F77-A7D4-F4BCC795D694Q33171188-C4DB1ED7-DB8B-4E26-9AD9-3DA87772E2E3Q33171299-40E6C5BA-9E8B-4E37-9D1F-C79D8A9695A4Q33173085-A416D55A-6819-4E95-95B0-742ECE545C48Q33173270-692E2638-CBAF-4C2C-9F9B-3839D06F75B6Q33595231-794D243B-7255-474C-982A-2D87B7AD0C06Q33661027-4E6B5081-8576-4704-A4AF-8F694AB53198Q34044611-68095246-D3E8-4C64-839D-81C78B106F26Q34389321-2E06FAE0-29E7-48C7-A70D-A870D8BA69AAQ36659539-397B98B1-D0A6-447B-A12C-4DED4B265472Q36659743-FEF9706E-03EF-4B5F-B0E2-DBD25C1C6722Q36931773-6E2B9614-BE62-4E47-86A8-5B4BA55C71DCQ37613089-26237DDC-816A-4082-BFF7-BDEAC231E6F5Q38027010-DC6C24EF-5244-4C52-8BD3-B480F2A1C12FQ38364307-02B01C74-2EA9-48F4-9A04-D43EB5FA67F0Q39996944-B7C70D40-6D24-4794-94FA-773E6D155E7AQ40058650-915D7E5C-5E67-4EAC-98D1-1ABC95FBF74CQ40386926-59F0D217-C328-40A1-AFAB-29E6F9808890Q41746723-75F9238C-0486-49D4-A3D6-304EA913D9D4Q48276367-9FCF7EF7-4CEE-4776-A03C-5430345560B7
P2860
GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).
description
1964 nî lūn-bûn
@nan
1964 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1964 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1964年の論文
@ja
1964年論文
@yue
1964年論文
@zh-hant
1964年論文
@zh-hk
1964年論文
@zh-mo
1964年論文
@zh-tw
1964年论文
@wuu
name
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@ast
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@en
type
label
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@ast
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@en
prefLabel
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@ast
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@en
P2093
P1476
GENETICAL ASPECTS OF THE CARDI ...... OCARDIOGRAPHIC ABNORMALITIES).
@en
P2093
P2860
P304
P356
10.1111/J.1469-1809.1964.TB00469.X
P407
P577
1964-11-01T00:00:00Z