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Results 1 - 10 of 323 for LM 10
  1. Surfactant dysfunction 
    ... Nov 16. Citation on PubMed Gower WA, Nogee LM. Surfactant dysfunction. Paediatr Respir Rev. 2011 Dec;12(4):223-9. doi: 10.1016/j.prrv.2011.01.005. Epub 2011 ...
    https://medlineplus.gov/genetics/condition/surfactant-dysfunction - Genetics
  2. Nonbullous congenital ichthyosiform erythroderma 
    ... AUTOSOMAL RECESSIVE 9; ARCI9 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10 PubMed Boyden LM, Craiglow BG, Hu RH, Zhou J, Browning J, ... L, Uitto J, Lifton RP, Paller AS, Milstone LM, Choate KA. Phenotypic spectrum of ... 2017 Jul;177(1):319-322. doi: 10.1111/bjd.15570. Epub 2017 Jun 7. No ...
    https://medlineplus.gov/...ous-congenital-ichthyosiform-erythroderma - Genetics
  3. Hereditary sensory and autonomic neuropathy type V 
    ... Nov 8. Citation on PubMed Lewin GR, Mendell LM. Nerve growth factor and nociception. Trends Neurosci. 1993 Sep;16(9):353-9. doi: 10.1016/0166-2236(93)90092-z. Citation on ...
    https://medlineplus.gov/...y-sensory-and-autonomic-neuropathy-type-v - Genetics
  4. NGF gene 
    ... Nov 8. Citation on PubMed Lewin GR, Mendell LM. Nerve growth factor and nociception. Trends Neurosci. 1993 Sep;16(9):353-9. doi: 10.1016/0166-2236(93)90092-z. Citation on ...
    https://medlineplus.gov/genetics/gene/ngf - Genetics
  5. PKHD1 gene 
    ... 75-85. doi: 10.1016/j.ymgme.2003.10.010. Citation on PubMed Lina F, Satlinb LM. Polycystic kidney disease: the cilium as a common ... Onuchic LF, Somlo S, Germino GG, Guay-Woodford LM. Comprehensive genomic analysis of ... doi: 10.1136/jmg.2004.024489. No abstract available. Citation ...
    https://medlineplus.gov/genetics/gene/pkhd1 - Genetics
  6. Parkinson's disease 
    ... 05.009. Citation on PubMed Tan EK, Skipper LM. Pathogenic mutations in Parkinson disease. Hum Mutat. 2007 Jul;28(7):641-53. doi: 10.1002/humu.20507. Citation on PubMed Van Den ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  7. Horner syndrome 
    ... Free article on PubMed Central Walton KA, Buono LM. Horner syndrome. Curr Opin Ophthalmol. 2003 Dec;14(6):357-63. doi: 10.1097/00055735-200312000-00007. Citation on PubMed Wang ...
    https://medlineplus.gov/genetics/condition/horner-syndrome - Genetics
  8. Floating-Harbor syndrome 
    ... MCD.0b013e32834af5a7. Citation on PubMed Asseidat I, Kaufman LM. Ocular abnormalities in Floating-Harbor syndrome. J AAPOS. 2009 Apr;13(2):218-20. doi: 10.1016/j.jaapos.2008.11.002. Citation on ...
    https://medlineplus.gov/genetics/condition/floating-harbor-syndrome - Genetics
  9. Lymphangioleiomyomatosis 
    ... Epub 2012 Sep 21. Citation on PubMed Moir LM. Lymphangioleiomyomatosis: Current understanding and potential treatments. Pharmacol Ther. 2016 Feb;158:114-24. doi: 10.1016/j.pharmthera.2015.12.008. Epub 2015 ...
    https://medlineplus.gov/genetics/condition/lymphangioleiomyomatosis - Genetics
  10. NR0B1 gene 
    ... 2003 May 1;12(9):1063-72. doi: 10.1093/hmg/ddg108. Citation on PubMed Ludbrook LM, Harley VR. Sex determination: a 'window' of DAX1 activity. Trends Endocrinol Metab. 2004 Apr;15(3):116-21. doi: 10.1016/j.tem.2004.02.002. Citation on ...
    https://medlineplus.gov/genetics/gene/nr0b1 - Genetics
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