-
1
-
-
17644363081
-
ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005
-
American Thoracic Society, European Respiratory Society (2005) ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005. Am J Respir Crit Care Med 171:912-930
-
(2005)
Am J Respir Crit Care Med
, vol.171
, pp. 912-930
-
-
Thoracic Society, A.1
Respiratory Society, E.2
-
3
-
-
73249125649
-
Primary ciliary dyskinesia: A consensus statement on diagnostic and treatment approaches in children
-
Barbato A, Frischer T, Kuehni CE, et al. (2009) Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children. Eur Respir J 34(6):1264-1276
-
(2009)
Eur Respir J
, vol.34
, Issue.6
, pp. 1264-1276
-
-
Barbato, A.1
Frischer, T.2
Kuehni, C.E.3
-
4
-
-
78651254549
-
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation
-
Becker-Heck A, Zohn IE, Okabe N, et al. (2011) The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nat Genet 43:79-84
-
(2011)
Nat Genet
, vol.43
, pp. 79-84
-
-
Becker-Heck, A.1
Zohn, I.E.2
Okabe, N.3
-
5
-
-
84864017587
-
The impact of hypertonic saline inhalation on mucociliary clearance and nasal nitric oxide
-
Bencova A, Vidan J, Rozborilova E, et al. (2012) The impact of hypertonic saline inhalation on mucociliary clearance and nasal nitric oxide. J Physiol Pharmacol 63:309-313
-
(2012)
J Physiol Pharmacol
, vol.63
, pp. 309-313
-
-
Bencova, A.1
Vidan, J.2
Rozborilova, E.3
-
6
-
-
33746990273
-
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome
-
DOI 10.1007/s00439-006-0210-5
-
Budny B, Chen W, Omran H, et al. (2006) A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome. Hum Genet 120:171-178 (Pubitemid 44204005)
-
(2006)
Human Genetics
, vol.120
, Issue.2
, pp. 171-178
-
-
Budny, B.1
Chen, W.2
Omran, H.3
Fliegauf, M.4
Tzschach, A.5
Wisniewska, M.6
Jensen, L.R.7
Raynaud, M.8
Shoichet, S.A.9
Badura, M.10
Lenzner, S.11
Latos-Bielenska, A.12
Ropers, H.-H.13
-
7
-
-
62649153946
-
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities
-
Castleman VH, Romio L, Chodhari R, et al. (2009) Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities. Am J Hum Genet 84:197-209
-
(2009)
Am J Hum Genet
, vol.84
, pp. 197-209
-
-
Castleman, V.H.1
Romio, L.2
Chodhari, R.3
-
8
-
-
0034111760
-
Analysis of ciliary beat pattern and beat frequency using digital high speed imaging: Comparison with the photomultiplier and photodiode methods
-
Chilvers MA, OCallaghan C (2000) Analysis of ciliary beat pattern and beat frequency using digital high speed imaging: comparison with the photomultiplier and photodiode methods. Thorax 55:314-317
-
(2000)
Thorax
, vol.55
, pp. 314-317
-
-
Ma, C.1
Ocallaghan, C.2
-
9
-
-
0042235314
-
Ciliary beat pattern is associated with specific ultrastructural defects in primary ciliary dyskinesia
-
DOI 10.1016/S0091-6749(03)01799-8
-
Chilvers MA, Rutman A, OCallaghan C (2003) Ciliary beat pattern is associated with specific ultrastructural defects in primary ciliary dyskinesia. J Allergy Clin Immunol 112(3):518-524 (Pubitemid 37108555)
-
(2003)
Journal of Allergy and Clinical Immunology
, vol.112
, Issue.3
, pp. 518-524
-
-
Chilvers, M.A.1
Rutman, A.2
O'Callaghan, C.3
-
10
-
-
0037385839
-
Functional analysis of cilia and ciliated epithelial ultrastructure in healthy children and young adults
-
DOI 10.1136/thorax.58.4.333
-
Chilvers MA, Rutman A, OCallaghan C (2003) Functional analysis of cilia and ciliated epithelial ultrastructure in healthy children and young adults. Thorax 58:333-338 (Pubitemid 36411420)
-
(2003)
Thorax
, vol.58
, Issue.4
, pp. 333-338
-
-
Chilvers, M.A.1
Rutman, A.2
O'Callaghan, C.3
-
11
-
-
0036062162
-
Primary ciliary dyskinesia: Age at diagnosis and symptom history
-
DOI 10.1080/080352502760069089
-
Coren ME, Meeks M, Morrison I, et al. (2002) Primary ciliary dyskinesia: age at diagnosis and symptom history. Acta Paediatr 91:667-669 (Pubitemid 34779328)
-
(2002)
Acta Paediatrica, International Journal of Paediatrics
, vol.91
, Issue.6
, pp. 667-669
-
-
Coren, M.E.1
Meeks, M.2
Morrison, I.3
Buchdahl, R.M.4
Bush, A.5
-
12
-
-
33847678960
-
A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia
-
DOI 10.1073/pnas.0611405104
-
Duriez B, Duquesnoy P, Escusier E, et al. (2007) A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia. Proc Natl Acad Sci USA 104:3336-3341 (Pubitemid 46364160)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.9
, pp. 3336-3341
-
-
Duriez, B.1
Duquesnoy, P.2
Escudier, E.3
Bridoux, A.-M.4
Escalier, D.5
Rayet, I.6
Marcos, E.7
Vojtek, A.-M.8
Bercher, J.-F.9
Amselem, S.10
-
13
-
-
38849086704
-
-
Ferkol T, Mitchison HM, OCallaghan C, et al. (2006) Chapter 16. Current issues in the basic mechanisms, pathophysiology, diagnosis and management of primary ciliary dyskinesia. Respiratory diseases in infants and children. Eur Respir Soc Mon 37:291-313
-
(2006)
Chapter 16. Current Issues in the Basic Mechanisms, Pathophysiology, Diagnosis and Management of Primary Ciliary Dyskinesia. Respiratory Diseases in Infants and Children. Eur Respir Soc Mon
, vol.37
, pp. 291-313
-
-
Ferkol, T.1
Mitchison, H.M.2
Ocallaghan, C.3
-
14
-
-
20444364841
-
Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia
-
DOI 10.1164/rccm.200411-1583OC
-
Fliegauf M, Olbrich H, Horvath J, et al. (2005) Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia. Am J Respir Crit Care Med 171(12):1343-1349 (Pubitemid 40800505)
-
(2005)
American Journal of Respiratory and Critical Care Medicine
, vol.171
, Issue.12
, pp. 1343-1349
-
-
Fliegauf, M.1
Olbrich, H.2
Horvath, J.3
Wildhaber, J.H.4
Zariwala, M.A.5
Kennedy, M.6
Knowles, M.R.7
Omran, H.8
-
15
-
-
84867259922
-
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia
-
Horani A, Druley TE, Zariwala MA, et al. (2012) Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia. Am J Hum Genet 91:685-693
-
(2012)
Am J Hum Genet
, vol.91
, pp. 685-693
-
-
Horani, A.1
Druley, T.E.2
Zariwala, M.A.3
-
16
-
-
84904637936
-
Nasal NO measurement in preschool children: Feasibility and validation of a tidal breathing technique via a resistance tube. 33
-
Graz
-
Jung A, Geidel C, Moeller A, et al. (2011) Nasal NO measurement in preschool children: feasibility and validation of a tidal breathing technique via a resistance tube. 33. Jahrestagung der Gesellschaft für pädiatrische Pneumologie, Graz
-
(2011)
Jahrestagung der Gesellschaft für Pädiatrische Pneumologie
-
-
Jung, A.1
Geidel, C.2
Moeller, A.3
-
17
-
-
0032765146
-
Nasal and lower airway level of nitric oxide in children with primary ciliary dyskinesia
-
DOI 10.1034/j.1399-3003.1999.13f28.x
-
Karadag B, James AJ, Gültekin E, et al. (1999) Nasal and lower airway level of nitric oxide in children with primary ciliary dyskinesia. Eur Respir J 13:1402-1405 (Pubitemid 29357160)
-
(1999)
European Respiratory Journal
, vol.13
, Issue.6
, pp. 1402-1405
-
-
Karadag, B.1
James, A.J.2
Gultekin, E.3
Wilson, N.M.4
Bush, A.5
-
18
-
-
84872285578
-
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
-
Knowles MR, Leigh MW, Ostrowski LE, et al. (2013) Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia. Am J Hum Genet 92:99-106
-
(2013)
Am J Hum Genet
, vol.92
, pp. 99-106
-
-
Knowles, M.R.1
Leigh, M.W.2
Ostrowski, L.E.3
-
19
-
-
84868384681
-
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia
-
Kott E, Duquesnoy P, Copin B, et al. (2012) Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia. Am J Hum Genet 91:958-964
-
(2012)
Am J Hum Genet
, vol.91
, pp. 958-964
-
-
Kott, E.1
Duquesnoy, P.2
Copin, B.3
-
20
-
-
55249083702
-
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm
-
Loges NT, Olbrich H, Fenske L, et al. (2008) DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm. Am J Hum Genet 83(5):547-558
-
(2008)
Am J Hum Genet
, vol.83
, Issue.5
, pp. 547-558
-
-
Loges, N.T.1
Olbrich, H.2
Fenske, L.3
-
21
-
-
71149086940
-
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects
-
Loges NT, Olbrich H, Becker-Heck A, et al. (2009) Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. Am J Hum Genet 85:883-889
-
(2009)
Am J Hum Genet
, vol.85
, pp. 883-889
-
-
Loges, N.T.1
Olbrich, H.2
Becker-Heck, A.3
-
22
-
-
0028023991
-
Primarily nasal origin of exhaled nitric oxide and absence in Kartagener's syndrome
-
Lundberg JO, Weitzberg E, Nordvall SL, et al. (1994) Primarily nasal origin of exhaled nitric oxide and absence in Kartageners syndrome. Eur Respir J 7:1501-1504 (Pubitemid 24268339)
-
(1994)
European Respiratory Journal
, vol.7
, Issue.8
, pp. 1501-1504
-
-
Lundberg, J.O.N.1
Weitzberg, E.2
Nordvall, S.L.3
Kuylenstierna, R.4
Lundberg, J.M.5
Alving, K.6
-
23
-
-
80051801443
-
Diagnostic value of nasal nitric oxide measured with non-velum closure techniques for children with primary ciliary dyskinesia
-
Mateos-Corral D, Coombs R, Grasemann H, et al. (2011) Diagnostic value of nasal nitric oxide measured with non-velum closure techniques for children with primary ciliary dyskinesia. J Pediatr 159:420-424
-
(2011)
J Pediatr
, vol.159
, pp. 420-424
-
-
Mateos-Corral, D.1
Coombs, R.2
Grasemann, H.3
-
24
-
-
79955856801
-
Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1
-
Mazor M, Alkrinawi S, Chalifa-Caspi V, et al. (2011) Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1. Am J Hum Genet 88:599-607
-
(2011)
Am J Hum Genet
, vol.88
, pp. 599-607
-
-
Mazor, M.1
Alkrinawi, S.2
Chalifa-Caspi, V.3
-
25
-
-
78651260210
-
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs
-
Merveille AC, Davis EE, Becker-Heck A, et al. (2011) CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet 43:72-78
-
(2011)
Nat Genet
, vol.43
, pp. 72-78
-
-
Merveille, A.C.1
Davis, E.E.2
Becker-Heck, A.3
-
26
-
-
84859436123
-
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia
-
Mitchison HM, Schmidts N, Loges NT, et al. (2012) Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia. Nat Genet 44:381-389
-
(2012)
Nat Genet
, vol.44
, pp. 381-389
-
-
Mitchison, H.M.1
Schmidts, N.2
Loges, N.T.3
-
27
-
-
33645765214
-
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
-
Moore A, Escudier E, Roger G, et al. (2006) RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. J Med Genet 43:326-333
-
(2006)
J Med Genet
, vol.43
, pp. 326-333
-
-
Moore, A.1
Escudier, E.2
Roger, G.3
-
28
-
-
78751656315
-
Questionnaire to preselect patients with a high probability of primary ciliary dyskinesia
-
Noll EM, Rieger CH, Hamelmann E, et al. (2011) Questionnaire to preselect patients with a high probability of primary ciliary dyskinesia. Klin Padiatr 223(1):22-26
-
(2011)
Klin Padiatr
, vol.223
, Issue.1
, pp. 22-26
-
-
Noll, E.M.1
Rieger, C.H.2
Hamelmann, E.3
-
29
-
-
0442313529
-
Primary Ciliary Dyskinesia: Diagnostic and Phenotypic Features
-
Noone PG, Leigh MW, Sannuti A, et al. (2004) Primary ciliary dyskinesia: diagnostic and phenotypic features. Am J Respir Crit Care Med 169:459-467 (Pubitemid 38187117)
-
(2004)
American Journal of Respiratory and Critical Care Medicine
, vol.169
, Issue.4
, pp. 459-467
-
-
Noone, P.G.1
Leigh, M.W.2
Sannuti, A.3
Minnix, S.L.4
Carson, J.L.5
Hazucha, M.6
Zariwala, M.A.7
Knowles, M.R.8
-
30
-
-
80053061098
-
Inner dynein arm defects causing primary ciliary dyskinesia: Repeat testing required
-
OCallaghan C, Rutman A, Williams GM, et al. (2011) Inner dynein arm defects causing primary ciliary dyskinesia: repeat testing required. Eur Respir J 38(3):603-607
-
(2011)
Eur Respir J
, vol.38
, Issue.3
, pp. 603-607
-
-
Ocallaghan, C.1
Rutman, A.2
Williams, G.M.3
-
31
-
-
0036479029
-
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
-
Olbrich H, Häffner K, Kispert A, et al. (2002) Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. Nat Genet 30:143-144
-
(2002)
Nat Genet
, vol.30
, pp. 143-144
-
-
Olbrich, H.1
Häffner, K.2
Kispert, A.3
-
32
-
-
33646120587
-
Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia
-
DOI 10.1203/01.pdr.0000200809.21364.e2, PII 0000645020060300000014
-
Olbrich H, Horvath J, Fekete A, et al. (2006) Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia. Pediatr Res 59(3):418-422 (Pubitemid 43740081)
-
(2006)
Pediatric Research
, vol.59
, Issue.3
, pp. 418-422
-
-
Olbrich, H.1
Horvath, J.2
Fekete, A.3
Loges, N.T.4
Van's Gravesande, K.S.5
Blum, A.6
Hormann, K.7
Omran, H.8
-
33
-
-
84867244938
-
Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry
-
Olbrich H, Schmidts M, Werner C, et al. (2012) Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry. Am J Hum Genet 91(4):672-684
-
(2012)
Am J Hum Genet
, vol.91
, Issue.4
, pp. 672-684
-
-
Olbrich, H.1
Schmidts, M.2
Werner, C.3
-
34
-
-
57349137660
-
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins
-
Omran H, Kobayashi D, Olbrich H, et al. (2008) Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins. Nature 456:611-616
-
(2008)
Nature
, vol.456
, pp. 611-616
-
-
Omran, H.1
Kobayashi, D.2
Olbrich, H.3
-
35
-
-
84872342461
-
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia
-
Onoufriadis A, Paff T, Antony D, et al. (2013) Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia. Am J Hum Genet 92:88-98
-
(2013)
Am J Hum Genet
, vol.92
, pp. 88-98
-
-
Onoufriadis, A.1
Paff, T.2
Antony, D.3
-
36
-
-
84861640948
-
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms
-
Panizzi JR, Becker-Heck A, Castleman VH, et al. (2012) CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms. Nat Genet 44:714-719
-
(2012)
Nat Genet
, vol.44
, pp. 714-719
-
-
Panizzi, J.R.1
Becker-Heck, A.2
Castleman, V.H.3
-
37
-
-
77951953097
-
A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia
-
Papon JF, Coste A, Roudot-Thoraval F, et al. (2010) A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia. Eur Respir J 35:1057-1063
-
(2010)
Eur Respir J
, vol.35
, pp. 1057-1063
-
-
Papon, J.F.1
Coste, A.2
Roudot-Thoraval, F.3
-
38
-
-
0033365058
-
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 dyskinesia
-
DOI 10.1086/302683
-
Pennarun G, Escudier E, Chapelin C, et al. (1999) Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. Am J Hum Genet 65:1508-1519 (Pubitemid 30468663)
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.6
, pp. 1508-1519
-
-
Pennarun, G.1
Escudier, E.2
Chapelin, C.3
Bridoux, A.-M.4
Cacheux, V.5
Roger, G.6
Clement, A.7
Goossens, M.8
Amselem, S.9
Duriez, B.10
-
39
-
-
79953693564
-
Nasal nitric oxide and nitric oxide synthase expression in primary ciliary dyskinesia
-
Pfifferi M, Bush A, Maggi F, et al. (2011) Nasal nitric oxide and nitric oxide synthase expression in primary ciliary dyskinesia. Eur Respir J 37(3):572-577
-
(2011)
Eur Respir J
, vol.37
, Issue.3
, pp. 572-577
-
-
Pfifferi, M.1
Bush, A.2
Maggi, F.3
-
40
-
-
33947407259
-
Nasal nitric oxide in atypical primary ciliary dyskinesia
-
DOI 10.1378/chest.06-2472
-
Pfifferi M, Caramella D, Cangiotti AM, et al. (2007) Nasal oxide in atypical primary dyskinesia. Chest 131:870-873 (Pubitemid 46446883)
-
(2007)
Chest
, vol.131
, Issue.3
, pp. 870-873
-
-
Pifferi, M.1
Caramella, D.2
Cangiotti, A.M.3
Ragazzo, V.4
Macchia, P.5
Boner, A.L.6
-
42
-
-
38949108779
-
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations
-
DOI 10.1002/humu.20656
-
Schwabe GC, Hoffmann K, Loges NT, et al. (2008) Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. Hum Mutat 29:289-298 (Pubitemid 351240602)
-
(2008)
Human Mutation
, vol.29
, Issue.2
, pp. 289-298
-
-
Schwabe, G.C.1
Hoffmann, K.2
Loges, N.T.3
Birker, D.4
Rossier, C.5
De Santi, M.M.6
Olbrich, H.7
Fliegauf, M.8
Failly, M.9
Liebers, U.10
Collura, M.11
Gaedicke, G.12
Mundlos, S.13
Wahn, U.14
Blouin, J.-L.15
Niggemann, B.16
Omran, H.17
Antonarakis, S.E.18
Bartoloni, L.19
-
43
-
-
76149089851
-
Diagnostic testing of patients suspected of primary ciliary dyskinesia
-
Stannard WA, Chilvers MA, Rutman A, et al. (2010) Diagnostic testing of patients suspected of primary ciliary dyskinesia. Am J Respir Crit Care Med 181(4):307-314
-
(2010)
Am J Respir Crit Care Med
, vol.181
, Issue.4
, pp. 307-314
-
-
Stannard, W.A.1
Chilvers, M.A.2
Rutman, A.3
-
44
-
-
82055175860
-
Ultrastructural pathology of primary ciliary dyskinesia: Report about 125 cases in Germany
-
Theegarten D, Ebsen M (2011) Ultrastructural pathology of primary ciliary dyskinesia: report about 125 cases in Germany. Diagn Pathol 6:115
-
(2011)
Diagn Pathol
, vol.6
, pp. 115
-
-
Theegarten, D.1
Ebsen, M.2
-
45
-
-
84867113504
-
Nitric oxide in primary ciliary dyskinesia
-
Walker WT, Jackson CL, Lackie PM, et al. (2012) Nitric oxide in primary ciliary dyskinesia. Eur Respir J 40:1024-1032
-
(2012)
Eur Respir J
, vol.40
, pp. 1024-1032
-
-
Walker, W.T.1
Jackson, C.L.2
Lackie, P.M.3
-
46
-
-
84874658994
-
The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans
-
Wirschell M, Olbrich H, Werner C, et al. (2013) The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans. Nat Genet 45(3):262-268
-
(2013)
Nat Genet
, vol.45
, Issue.3
, pp. 262-268
-
-
Wirschell, M.1
Olbrich, H.2
Werner, C.3
-
47
-
-
84860261615
-
Efficacy of mometasone furoate nasal spray for nasal symptoms, quality of life, rhinitis-disturbed sleep, and nasal nitric oxide in patients with perennial allergic rhinitis
-
Yamada T, Yamamoto H, Kubo S, et al. (2012) Efficacy of mometasone furoate nasal spray for nasal symptoms, quality of life, rhinitis-disturbed sleep, and nasal nitric oxide in patients with perennial allergic rhinitis. Allergy Asthma Proc 33:e9-e16
-
(2012)
Allergy Asthma Proc
, vol.33
-
-
Yamada, T.1
Yamamoto, H.2
Kubo, S.3
|