{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,26]],"date-time":"2026-03-26T23:41:01Z","timestamp":1774568461412,"version":"3.50.1"},"reference-count":13,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2020,1,23]],"date-time":"2020-01-23T00:00:00Z","timestamp":1579737600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2020,1,23]],"date-time":"2020-01-23T00:00:00Z","timestamp":1579737600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Acta Neurol Belg"],"published-print":{"date-parts":[[2020,2]]},"DOI":"10.1007\/s13760-020-01275-9","type":"journal-article","created":{"date-parts":[[2020,1,23]],"date-time":"2020-01-23T10:02:55Z","timestamp":1579773775000},"page":"149-154","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Hereditary axonal neuropathy related to MME gene mutation in a family with fetomaternal alloimmune glomerulonephritis"],"prefix":"10.1007","volume":"120","author":[{"given":"M.","family":"Dupuis","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4377-8966","authenticated-orcid":false,"given":"J. M.","family":"Raymackers","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N.","family":"Ackermans","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Boulanger","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Verellen-Dumoulin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2020,1,23]]},"reference":[{"key":"1275_CR1","doi-asserted-by":"publisher","first-page":"659","DOI":"10.1002\/ana.24612","volume":"79","author":"Y Higuchi","year":"2016","unstructured":"Higuchi Y, Hashiguchi A, Yuan J et al (2016) Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2. Ann Neurol 79:659\u2013672","journal-title":"Ann Neurol"},{"key":"1275_CR2","doi-asserted-by":"publisher","first-page":"607","DOI":"10.1016\/j.ajhg.2016.07.008","volume":"99","author":"M Auer-Grumbach","year":"2016","unstructured":"Auer-Grumbach M, Toegel S, Schabhuttl M et al (2016) Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies. Am J Hum Genet 99:607\u2013623","journal-title":"Am J Hum Genet"},{"key":"1275_CR3","doi-asserted-by":"publisher","first-page":"2053","DOI":"10.1056\/NEJMoa012895","volume":"346","author":"H Debiec","year":"2002","unstructured":"Debiec H, Guigonis V, Mougenot M et al (2002) Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies. N Engl J Med 346:2053\u20132060","journal-title":"N Engl J Med"},{"key":"1275_CR4","doi-asserted-by":"publisher","first-page":"1252","DOI":"10.1016\/S0140-6736(04)17142-0","volume":"364","author":"H Debiec","year":"2004","unstructured":"Debiec H, Nauta J, Coulet F et al (2004) Role of truncating mutations in MME gene in foetomaternal alloimmunisation and antenatal glomerulopathies. Lancet 364:1252\u20131259","journal-title":"Lancet"},{"key":"1275_CR5","doi-asserted-by":"publisher","first-page":"1399","DOI":"10.1007\/s00467-006-0203-6","volume":"21","author":"JL Nortier","year":"2006","unstructured":"Nortier JL, Debiec H, Tournay Y et al (2006) Neonatal disease in neutral endopeptidase alloimmunization: lessons for immunological monitoring. Pediatr Nephrol 21:1399\u20131405","journal-title":"Pediatr Nephrol"},{"key":"1275_CR6","doi-asserted-by":"publisher","first-page":"60","DOI":"10.1016\/j.jns.2017.08.227","volume":"381","author":"N Ackermans","year":"2017","unstructured":"Ackermans N, Dupuis M, Raymackers JM et al (2017) Hereditary motor and sensory neuropathy (HMSN) and foeto-maternal autoimmune glomerulopathy coexist in members of a family harbouring metallo-membrane-endopeptidase (MME) gene mutation. J Neurol Sci 381:60","journal-title":"J Neurol Sci"},{"key":"1275_CR7","doi-asserted-by":"publisher","first-page":"814","DOI":"10.1136\/jmedgenet-2018-105650","volume":"55","author":"V Lupo","year":"2018","unstructured":"Lupo V, Frasquet M, S\u00e1nchez-Monteagudo A et al (2018) Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations. J Med Genet 55:814\u2013823","journal-title":"J Med Genet"},{"key":"1275_CR8","doi-asserted-by":"publisher","first-page":"177","DOI":"10.1016\/j.nbd.2008.11.002","volume":"35","author":"HH Kr\u00e4mer","year":"2009","unstructured":"Kr\u00e4mer HH, Le H, Lu B et al (2009) Increased pain and neurogenic inflammation in mice deficient of neutral endopeptidase. Neurobiol Dis 35:177\u2013183","journal-title":"Neurobiol Dis"},{"key":"1275_CR9","doi-asserted-by":"publisher","first-page":"574","DOI":"10.1016\/j.pain.2013.12.003","volume":"155","author":"L He","year":"2014","unstructured":"He L, \u00dc\u00e7eyler N, Kr\u00e4mer HH et al (2014) Methylprednisolone prevents nerve injury-induced hyperalgesia in neprilysin knockout mice. Pain 155:574\u2013580","journal-title":"Pain"},{"key":"1275_CR10","doi-asserted-by":"crossref","first-page":"1990","DOI":"10.1002\/glia.23680","volume":"67","author":"I Cervellini","year":"2019","unstructured":"Cervellini I, Galino J, Zhu N et al (2019) Membrane metallo-endopeptidase is dispensable for repair after nerve injury. Glia 67:1990\u20132000","journal-title":"Glia"},{"key":"1275_CR11","doi-asserted-by":"publisher","first-page":"e94","DOI":"10.1212\/NXG.0000000000000094","volume":"2","author":"C Depondt","year":"2016","unstructured":"Depondt C, Donatello S, Rai M et al (2016) MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43). Neurol Genet 2:e94","journal-title":"Neurol Genet"},{"key":"1275_CR12","doi-asserted-by":"publisher","first-page":"1728","DOI":"10.1002\/acn3.50868","volume":"6","author":"D Hong","year":"2019","unstructured":"Hong D, Fang P, Yao S et al (2019) Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy. Ann Clin Transl Neurol 6:1728\u20131738","journal-title":"Ann Clin Transl Neurol"},{"key":"1275_CR13","doi-asserted-by":"publisher","first-page":"539","DOI":"10.1056\/NEJMoa1812851","volume":"380","author":"E Velazquez","year":"2019","unstructured":"Velazquez E, Morrow D, DeVore A et al (2019) Angiotensin-neprilysin inhibition in acute decompensated heart failure. N Engl J Med 380:539\u2013548","journal-title":"N Engl J Med"}],"container-title":["Acta Neurologica Belgica"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s13760-020-01275-9.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s13760-020-01275-9\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s13760-020-01275-9.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,25]],"date-time":"2023-09-25T14:45:59Z","timestamp":1695653159000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s13760-020-01275-9"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,1,23]]},"references-count":13,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2020,2]]}},"alternative-id":["1275"],"URL":"https:\/\/doi.org\/10.1007\/s13760-020-01275-9","relation":{},"ISSN":["0300-9009","2240-2993"],"issn-type":[{"value":"0300-9009","type":"print"},{"value":"2240-2993","type":"electronic"}],"subject":[],"published":{"date-parts":[[2020,1,23]]},"assertion":[{"value":"19 June 2019","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"7 January 2020","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"23 January 2020","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}]}}