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Assessment of ventricular function in arterial hypertension with radionuclide ventriculography. [electronic resource] by
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- Albertini, A
- Alli, C
- Canciani, C
- Di Tullio, M
- Manzini, M
- Mariotti, G
- Salmoirago, E
- Taioli, E
- Zatta, G
Producer: 19890302
In:
The American journal of medicine vol. 84
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24.
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Arm position as a source of error in blood pressure measurement. [electronic resource] by
- Mariotti, G
- Alli, C
- Avanzini, F
- Canciani, C
- Di Tullio, M
- Manzini, M
- Salmoirago, E
- Taioli, E
- Zussino, A
- Radice, M
Producer: 19871125
In:
Clinical cardiology vol. 10
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25.
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Role of the laboratory in monitoring patients receiving dual antiplatelet therapy. [electronic resource] by
- Vidali, M
- Rolla, R
- Parrella, M
- Cassani, C
- Manzini, M
- Portalupi, M R
- Serino, R
- Prando, M D
- Bellomo, G
- Pergolini, P
Producer: 20130212
In:
International journal of laboratory hematology vol. 34
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26.
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[Usefulness of exertion tests in the evaluation of the effectiveness of antihypertensive therapy]. [electronic resource] by
- Radice, M
- Alli, C
- Avanzini, F
- Canciani, C
- Castelli, M R
- Di Tullio, M
- Giudici, V
- Manzini, M
- Mariotti, G
- Salmoirago, E
Producer: 19871029
In:
Giornale italiano di cardiologia vol. 17
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27.
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Abrogated Freud-1/Cc2d1a Repression of 5-HT1A Autoreceptors Induces Fluoxetine-Resistant Anxiety/Depression-Like Behavior. [electronic resource] by
- Vahid-Ansari, Faranak
- Daigle, Mireille
- Manzini, M Chiara
- Tanaka, Kenji F
- Hen, René
- Geddes, Sean D
- Béïque, Jean-Claude
- James, Jonathan
- Merali, Zul
- Albert, Paul R
Producer: 20171215
In:
The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 37
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28.
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Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556. [electronic resource] by
- Cauley, Edmund S
- Hamed, Ahlam
- Mohamed, Inaam N
- Elseed, Maha
- Martinez, Samantha
- Yahia, Ashraf
- Abozar, Fatima
- Abubakr, Rayan
- Koko, Mahmoud
- Elsayed, Liena
- Piao, Xianhua
- Salih, Mustafa A
- Manzini, M Chiara
Producer: 20200106
In:
Neurogenetics vol. 20
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29.
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COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans. [electronic resource] by
- Labelle-Dumais, Cassandre
- Dilworth, David J
- Harrington, Emily P
- de Leau, Michelle
- Lyons, David
- Kabaeva, Zhyldyz
- Manzini, M Chiara
- Dobyns, William B
- Walsh, Christopher A
- Michele, Daniel E
- Gould, Douglas B
Producer: 20110912
In:
PLoS genetics vol. 7
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30.
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A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish. [electronic resource] by
- Gupta, Vandana A
- Kawahara, Genri
- Myers, Jennifer A
- Chen, Aye T
- Hall, Thomas E
- Manzini, M Chiara
- Currie, Peter D
- Zhou, Yi
- Zon, Leonard I
- Kunkel, Louis M
- Beggs, Alan H
Producer: 20130219
In:
PloS one vol. 7
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Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2. [electronic resource] by
- Di Blasi, Claudia
- Bellafiore, Emanuela
- Salih, Mustafa Am
- Manzini, M Chiara
- Moore, Steven A
- Seidahmed, Mohammed Z
- Mukhtar, Maowia M
- Karrar, Zein A
- Walsh, Christopher A
- Campbell, Kevin P
- Mantegazza, Renato
- Morandi, Lucia
- Mora, Marina
Producer: 20121002
In:
BMC research notes vol. 4
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32.
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Developmental and degenerative features in a complicated spastic paraplegia. [electronic resource] by
- Manzini, M Chiara
- Rajab, Anna
- Maynard, Thomas M
- Mochida, Ganeshwaran H
- Tan, Wen-Hann
- Nasir, Ramzi
- Hill, R Sean
- Gleason, Danielle
- Al Saffar, Muna
- Partlow, Jennifer N
- Barry, Brenda J
- Vernon, Mike
- LaMantia, Anthony-Samuel
- Walsh, Christopher A
Producer: 20100514
In:
Annals of neurology vol. 67
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33.
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Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social Deficits. [electronic resource] by
- Oaks, Adam W
- Zamarbide, Marta
- Tambunan, Dimira E
- Santini, Emanuela
- Di Costanzo, Stefania
- Pond, Heather L
- Johnson, Mark W
- Lin, Jeff
- Gonzalez, Dilenny M
- Boehler, Jessica F
- Wu, Guangying K
- Klann, Eric
- Walsh, Christopher A
- Manzini, M Chiara
Producer: 20180306
In:
Cerebral cortex (New York, N.Y. : 1991) vol. 27
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POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations. [electronic resource] by
- Di Costanzo, Stefania
- Balasubramanian, Anuradha
- Pond, Heather L
- Rozkalne, Anete
- Pantaleoni, Chiara
- Saredi, Simona
- Gupta, Vandana A
- Sunu, Christine M
- Yu, Timothy W
- Kang, Peter B
- Salih, Mustafa A
- Mora, Marina
- Gussoni, Emanuela
- Walsh, Christopher A
- Manzini, M Chiara
Producer: 20150610
In:
Human molecular genetics vol. 23
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Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B. [electronic resource] by
- Bione, S
- Rizzolio, F
- Sala, C
- Ricotti, R
- Goegan, M
- Manzini, M C
- Battaglia, R
- Marozzi, A
- Vegetti, W
- Dalprà, L
- Crosignani, P G
- Ginelli, E
- Nappi, R
- Bernabini, S
- Bruni, V
- Torricelli, F
- Zuffardi, O
- Toniolo, D
Producer: 20050531
In:
Human reproduction (Oxford, England) vol. 19
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36.
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Structure of the polyisoprenyl-phosphate glycosyltransferase GtrB and insights into the mechanism of catalysis. [electronic resource] by
- Ardiccioni, Chiara
- Clarke, Oliver B
- Tomasek, David
- Issa, Habon A
- von Alpen, Desiree C
- Pond, Heather L
- Banerjee, Surajit
- Rajashankar, Kanagalaghatta R
- Liu, Qun
- Guan, Ziqiang
- Li, Chijun
- Kloss, Brian
- Bruni, Renato
- Kloppmann, Edda
- Rost, Burkhard
- Manzini, M Chiara
- Shapiro, Lawrence
- Mancia, Filippo
Producer: 20160609
In:
Nature communications vol. 7
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37.
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Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East. [electronic resource] by
- Manzini, M Chiara
- Gleason, Danielle
- Chang, Bernard S
- Hill, R Sean
- Barry, Brenda J
- Partlow, Jennifer N
- Poduri, Annapurna
- Currier, Sophie
- Galvin-Parton, Patricia
- Shapiro, Lawrence R
- Schmidt, Karen
- Davis, Jessica G
- Basel-Vanagaite, Lina
- Seidahmed, Mohamed Z
- Salih, Mustafa A M
- Dobyns, William B
- Walsh, Christopher A
Producer: 20081211
In:
Human mutation vol. 29
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38.
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CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasis. [electronic resource] by
- Manzini, M Chiara
- Xiong, Lan
- Shaheen, Ranad
- Tambunan, Dimira E
- Di Costanzo, Stefania
- Mitisalis, Vanessa
- Tischfield, David J
- Cinquino, Antonella
- Ghaziuddin, Mohammed
- Christian, Mehtab
- Jiang, Qin
- Laurent, Sandra
- Nanjiani, Zohair A
- Rasheed, Saima
- Hill, R Sean
- Lizarraga, Sofia B
- Gleason, Danielle
- Sabbagh, Diya
- Salih, Mustafa A
- Alkuraya, Fowzan S
- Walsh, Christopher A
Producer: 20150824
In:
Cell reports vol. 8
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39.
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Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome. [electronic resource] by
- Manzini, M Chiara
- Tambunan, Dimira E
- Hill, R Sean
- Yu, Tim W
- Maynard, Thomas M
- Heinzen, Erin L
- Shianna, Kevin V
- Stevens, Christine R
- Partlow, Jennifer N
- Barry, Brenda J
- Rodriguez, Jacqueline
- Gupta, Vandana A
- Al-Qudah, Abdel-Karim
- Eyaid, Wafaa M
- Friedman, Jan M
- Salih, Mustafa A
- Clark, Robin
- Moroni, Isabella
- Mora, Marina
- Beggs, Alan H
- Gabriel, Stacey B
- Walsh, Christopher A
Producer: 20121217
In:
American journal of human genetics vol. 91
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40.
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Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy. [electronic resource] by
- Osborn, Daniel P S
- Pond, Heather L
- Mazaheri, Neda
- Dejardin, Jeremy
- Munn, Christopher J
- Mushref, Khaloob
- Cauley, Edmund S
- Moroni, Isabella
- Pasanisi, Maria Barbara
- Sellars, Elizabeth A
- Hill, R Sean
- Partlow, Jennifer N
- Willaert, Rebecca K
- Bharj, Jaipreet
- Malamiri, Reza Azizi
- Galehdari, Hamid
- Shariati, Gholamreza
- Maroofian, Reza
- Mora, Marina
- Swan, Laura E
- Voit, Thomas
- Conti, Francesco J
- Jamshidi, Yalda
- Manzini, M Chiara
Producer: 20170510
In:
American journal of human genetics vol. 100
Availability: No items available.
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