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66181.
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66182.
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66183.
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66184.
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66185.
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A new ABCG2 null allele with a 27-kb deletion including the promoter region causing the Jr(a-) phenotype. [electronic resource] by
- Ogasawara, Kenichi
- Osabe, Takahiro
- Suzuki, Yumi
- Tsuneyama, Hatsue
- Isa, Kazumi
- Kawai, Miho
- Obara, Kumi
- Ogiyama, Yoshiko
- Ito, Shoichi
- Uchikawa, Makoto
- Satake, Masahiro
- Tadokoro, Kenji
Producer: 20150911
In:
Transfusion vol. 55
Availability: No items available.
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66186.
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66187.
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66188.
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66189.
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Development of a flow rate monitoring method for the wearable ventricular assist device driver. [electronic resource] by
- Ohnuma, Kentaro
- Homma, Akihiko
- Sumikura, Hirohito
- Tsukiya, Tomonori
- Takewa, Yoshiaki
- Mizuno, Toshihide
- Mukaibayashi, Hiroshi
- Kojima, Koichi
- Katano, Kazuo
- Taenaka, Yoshiyuki
- Tatsumi, Eisuke
Producer: 20160719
In:
Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs vol. 18
Availability: No items available.
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66190.
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66191.
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66192.
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66193.
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66194.
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66195.
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66196.
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Activating autoantibodies to the β1/2-adrenergic and M2 muscarinic receptors associate with atrial tachyarrhythmias in patients with hyperthyroidism. [electronic resource] by
- Galloway, Allison
- Li, Hongliang
- Vanderlinde-Wood, Megan
- Khan, Muneer
- Benbrook, Alexandria
- Liles, Campbell
- Zillner, Caitlin
- Rao, Veitla
- Cunningham, Madeleine W
- Yu, Xichun
- Kem, David C
Producer: 20160526
In:
Endocrine vol. 49
Availability: No items available.
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66197.
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Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study. [electronic resource] by
- Baş, Firdevs
- Uyguner, Z Oya
- Darendeliler, Feyza
- Aycan, Zehra
- Çetinkaya, Ergun
- Berberoğlu, Merih
- Şiklar, Zeynep
- Öcal, Gönül
- Darcan, Şükran
- Gökşen, Damla
- Topaloğlu, Ali Kemal
- Yüksel, Bilgin
- Özbek, Mehmet Nuri
- Ercan, Oya
- Evliyaoğlu, Olcay
- Çetinkaya, Semra
- Şen, Yaşar
- Atabek, Emre
- Toksoy, Güven
- Aydin, Banu Küçükemre
- Bundak, Rüveyde
Producer: 20160526
In:
Endocrine vol. 49
Availability: No items available.
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66198.
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Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption. [electronic resource] by
- Erlacher, Miriam
- Grünert, Sarah Catharina
- Cseh, Annamaria
- Steinfeld, Robert
- Salzer, Ulrich
- Lausch, Ekkehart
- Nosswitz, Ulrike
- Dückers, Gregor
- Niehues, Tim
- Ehl, Stephan
- Niemeyer, Charlotte Marie
- Speckmann, Carsten
Producer: 20150728
In:
Pediatric blood & cancer vol. 62
Availability: No items available.
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66199.
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66200.
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