Hasil Pencarian - Yulia Rodina
- Menampilkan 1 - 16 hasil dari 16
-
1
What do asymmetries in children’s performance tell us about the nature of their underlying knowledge? oleh Yulia Rodina
Diterbitkan 2008-02-01Dapatkan teks lengkap
Artikel -
2
Hvor mange genus er det i Trondheims-dialekten? oleh Guro Busterud, Terje Lohndal, Yulia Rodina, Marit Westergaard
Diterbitkan 2021-01-01Dapatkan teks lengkap
Artikel -
3
The Dative Alternation in Norwegian Child Language oleh Merete Anderssen, Paula Fikkert, Roksolana Mykhaylyk, Yulia Rodina
Diterbitkan 2012-05-01Dapatkan teks lengkap
Artikel -
4
Foreign Accent in Pre- and Primary School Heritage Bilinguals oleh Tanja Kupisch, Nadine Kolb, Yulia Rodina, Olga Urek
Diterbitkan 2021-05-01Dapatkan teks lengkap
Artikel -
5
-
6
-
7
Documenting heritage language experience using questionnaires oleh Aleksandra Tomić, Yulia Rodina, Fatih Bayram, Cécile De Cat, Cécile De Cat
Diterbitkan 2023-05-01Dapatkan teks lengkap
Artikel -
8
Internal and External Factors in Heritage Language Acquisition: Evidence From Heritage Russian in Israel, Germany, Norway, Latvia and the United Kingdom oleh Yulia Rodina, Tanja Kupisch, Tanja Kupisch, Natalia Meir, Natalia Mitrofanova, Olga Urek, Marit Westergaard, Marit Westergaard
Diterbitkan 2020-03-01Dapatkan teks lengkap
Artikel -
9
Morphological transparency and markedness matter in heritage speaker gender processing: an EEG study oleh Alicia Luque, Alicia Luque, Eleonora Rossi, Maki Kubota, Megan Nakamura, César Rosales, Cristina López-Rojas, Yulia Rodina, Jason Rothman, Jason Rothman
Diterbitkan 2023-06-01Dapatkan teks lengkap
Artikel -
10
Rituximab and Abatacept Are Effective in Differential Treatment of Interstitial Lymphocytic Lung Disease in Children With Primary Immunodeficiencies oleh Yulia Rodina, E. Deripapa, O. Shvets, A. Mukhina, A. Roppelt, D. Yuhacheva, A. Laberko, V. Burlakov, D. Abramov, G. Tereshchenko, G. Novichkova, Anna Shcherbina
Diterbitkan 2021-09-01Dapatkan teks lengkap
Artikel -
11
Combined therapy with IL-1 and JAK inhibitors in a patient with the NLRP1 gene mutation and a complex inflammatory phenotype oleh Vasily Burlakov, MD, Anna Kozlova, PhD, Dmitry Pershin, PhD, Yulia Rodina, MD, PhD, Igor Khamin, MD, Galina Novichkova, MD, PhD, Ivona Aksentijevich, PhD, Anna Shcherbina, MD, PhD
Diterbitkan 2024-08-01Dapatkan teks lengkap
Artikel -
12
Prospective Study of a Cohort of Russian Nijmegen Breakage Syndrome Patients Demonstrating Predictive Value of Low Kappa-Deleting Recombination Excision Circle (KREC) Numbers and B... oleh Elena Deripapa, Dmitry Balashov, Yulia Rodina, Alexandra Laberko, Natalya Myakova, Nataliia V. Davydova, Nataliia V. Davydova, Maria A. Gordukova, Dmitrii S. Abramov, Galina V. Pay, Larisa Shelikhova, Andrey P. Prodeus, Andrey P. Prodeus, Mikhail A. Maschan, Alexey A. Maschan, Anna Shcherbina
Diterbitkan 2017-07-01Dapatkan teks lengkap
Artikel -
13
A Rare Case of <i>TP63</i>-Associated Lymphopenia Revealed by Newborn Screening Using TREC oleh Andrey Marakhonov, Elena Serebryakova, Anna Mukhina, Anastasia Vechkasova, Nikolai Prokhorov, Irina Efimova, Natalia Balinova, Anastasia Lobenskaya, Tatyana Vasilyeva, Victoria Zabnenkova, Oxana Ryzhkova, Yulia Rodina, Dmitry Pershin, Nadezhda Soloveva, Anna Fomenko, Djamila Saydaeva, Aset Ibisheva, Taisiya Irbaieva, Alexander Koroteev, Rena Zinchenko, Sergey Voronin, Anna Shcherbina, Sergey Kutsev
Diterbitkan 2024-10-01Dapatkan teks lengkap
Artikel -
14
Decreased TREC and KREC levels in newborns with trisomy 21 oleh Andrey Marakhonov, Anna Mukhina, Elena Vlasova, Irina Efimova, Natalya Balinova, Yulia Rodina, Dmitry Pershin, Zhanna Markova, Marina Minzhenkova, Nadezhda Shilova, Dzhaina Mudaeva, Djamila Saydaeva, Taisiya Irbaieva, Svetlana Matulevich, Elena Belyashova, Grigoriy Yakubovskiy, Inna Tebieva, Yulia Gabisova, Murat Ikaev, Nataliya Irinina, Liya Nurgalieva, Elena Saifullina, Tatiana Belyaeva, Olga Romanova, Sergey Voronin, Rena Zinchenko, Anna Shcherbina, Sergey Kutsev
Diterbitkan 2024-10-01Dapatkan teks lengkap
Artikel -
15
Novel hemizygous CORO1A variant leads to combined immunodeficiency with defective platelet calcium signaling and cell mobility oleh Anna Khoreva, MD, Kirill R. Butov, MD, Elena I. Nikolaeva, MD, Alexey Martyanov, PhD, Elena Kulakovskaya, MD, Dmitry Pershin, MD, Maxim Alexenko, MD, Maria Kurnikova, MD, Ruslan Abasov, MD, Elena Raykina, PhD, Dmitry Abramov, MD, Kristina Arnaudova, PhD, Yulia Rodina, PhD, Natalia Trubina, MD, Yulia Skvortsova, PhD, Dmitry Balashov, PhD, Anastasia Sveshnikova, PhD, Alexey Maschan, PhD, Galina Novichkova, PhD, Mikhail Panteleev, PhD, Anna Shcherbina, PhD
Diterbitkan 2024-02-01Dapatkan teks lengkap
Artikel -
16
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation oleh Andrea Accogli, Saurabh Shakya, Taewoo Yang, Christine Insinna, Soo Yeon Kim, David Bell, Kirill R. Butov, Mariasavina Severino, Marcello Niceta, Marcello Scala, Hyun Sik Lee, Taekyeong Yoo, Jimmy Stauffer, Huijie Zhao, Chiara Fiorillo, Marina Pedemonte, Maria C. Diana, Simona Baldassari, Viktoria Zakharova, Anna Shcherbina, Yulia Rodina, Christina Fagerberg, Laura Sønderberg Roos, Jolanta Wierzba, Artur Dobosz, Amanda Gerard, Lorraine Potocki, Jill A. Rosenfeld, Seema R. Lalani, Tiana M. Scott, Daryl Scott, Mahshid S. Azamian, Raymond Louie, Hannah W. Moore, Neena L. Champaigne, Grace Hollingsworth, Annalaura Torella, Vincenzo Nigro, Rafal Ploski, Vincenzo Salpietro, Federico Zara, Simone Pizzi, Giovanni Chillemi, Marzia Ognibene, Erin Cooney, Jenny Do, Anders Linnemann, Martin J. Larsen, Suzanne Specht, Kylie J. Walters, Hee-Jung Choi, Murim Choi, Marco Tartaglia, Phillippe Youkharibache, Jong-Hee Chae, Valeria Capra, Sung-Gyoo Park, Christopher J. Westlake
Diterbitkan 2024-01-01Dapatkan teks lengkap
Artikel