Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Ip, Patrick
Knight, Ravi
Dokal, Inderjeet
Manzur, Adnan Y.
and
Muntoni, Francesco
2005.
Peripheral neuropathy—a novel finding in dyskeratosis congenita.
European Journal of Paediatric Neurology,
Vol. 9,
Issue. 2,
p.
85.
Marrone, Anna
Walne, Amanda
and
Dokal, Inderjeet
2005.
Dyskeratosis congenita: telomerase, telomeres and anticipation.
Current Opinion in Genetics & Development,
Vol. 15,
Issue. 3,
p.
249.
Walne, Amanda J.
Marrone, Anna
and
Dokal, Inderjeet
2005.
Dyskeratosis Congenita: A Disorder of Defective Telomere Maintenance?.
International Journal of Hematology,
Vol. 82,
Issue. 3,
p.
184.
Kanegane, Hirokazu
Kasahara, Yoshihito
Okamura, Jun
Hongo, Teruaki
Tanaka, Rieko
Nomura, Keiko
Kojima, Seiji
and
Miyawaki, Toshio
2005.
Identification of DKC1 gene mutations in Japanese patients with X‐linked dyskeratosis congenita.
British Journal of Haematology,
Vol. 129,
Issue. 3,
p.
432.
Alter, Blanche P.
2005.
Bone Marrow Failure: A Child Is Not Just a Small Adult (But an Adult Can Have a Childhood Disease).
Hematology,
Vol. 2005,
Issue. 1,
p.
96.
Jefford, Charles Edward
and
Irminger-Finger, Irmgard
2006.
Mechanisms of chromosome instability in cancers.
Critical Reviews in Oncology/Hematology,
Vol. 59,
Issue. 1,
p.
1.
Gomes, Mônica Fernandes
Abreu, Paula Pinheiro
Banzi, Éfani Caroline de Freitas
and
Nogueira, Terezinha de Oliveira
2006.
Interdisciplinary approach to treat dyskeratosis congenita associated with severe aplastic anemia: A case report.
Special Care in Dentistry,
Vol. 26,
Issue. 2,
p.
81.
Mahiques, L
Febrer, I
Vilata, JJ
and
Fortea, JM
2006.
A case of dyskeratosis congenita associated with schizophrenia and two malignancies.
Journal of the European Academy of Dermatology and Venereology,
Vol. 20,
Issue. 9,
p.
1159.
Lipton, Jeffrey M.
Atsidaftos, Eva
Zyskind, Israel
and
Vlachos, Adrianna
2006.
Improving clinical care and elucidating the pathophysiology of Diamond Blackfan anemia: An update from the Diamond Blackfan Anemia Registry.
Pediatric Blood & Cancer,
Vol. 46,
Issue. 5,
p.
558.
Lipton, Jeffrey M.
2006.
Diamond Blackfan Anemia: New Paradigms for a “Not So Pure” Inherited Red Cell Aplasia.
Seminars in Hematology,
Vol. 43,
Issue. 3,
p.
167.
Marrone, Anna
and
Dokal, Inderjeet
2006.
Dyskeratosis congenita: a disorder of telomerase deficiency and its relationship to other diseases.
Expert Review of Dermatology,
Vol. 1,
Issue. 3,
p.
463.
Arceci, Robert J.
2007.
Acute Myelogenous Leukemia.
p.
345.
Simeoni, Sara
Puccetti, Antonio
Chilosi, Marco
Tinazzi, Elisa
Prati, Daniele
Corrocher, Roberto
and
Lunardi, Claudio
2007.
Type 1 neurofibromatosis complicated by pulmonary artery hypertension: a case report.
The Journal of Medical Investigation,
Vol. 54,
Issue. 3,4,
p.
354.
Yamaguchi, Hiroki
2007.
Mutations of Telomerase Complex Genes Linked to Bone Marrow Failures.
Journal of Nippon Medical School,
Vol. 74,
Issue. 3,
p.
202.
Saez-De-Ocariz, Marimar
Orozco-Covarrubias, Luz
Durán-McKinster, Carola
and
Ruiz-Maldonado, Ramón
2008.
Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes.
p.
661.
Du, Hong-Yan
Bessler, Monica
and
Mason, Philip J.
2008.
Telomeres and Telomerase in Ageing, Disease, and Cancer.
p.
77.
Savage, Sharon A.
Giri, Neelam
Baerlocher, Gabriela M.
Orr, Nick
Lansdorp, Peter M.
and
Alter, Blanche P.
2008.
TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita.
The American Journal of Human Genetics,
Vol. 82,
Issue. 2,
p.
501.
Kirwan, M
and
Dokal, I
2008.
Dyskeratosis congenita: a genetic disorder of many faces.
Clinical Genetics,
Vol. 73,
Issue. 2,
p.
103.
Hamidah, Alias
Rashid, Radhiyah Abdul
Jamal, Rahman
Zhao, Meina
and
Kanegane, Hirokazu
2008.
X‐linked dyskeratosis congenita in Malaysia.
Pediatric Blood & Cancer,
Vol. 50,
Issue. 2,
p.
432.
Aslan, Deniz
Ozdek, Sengul
Camurdan, Orhun
Bideci, Aysun
and
Cinaz, Peyami
2009.
Dyskeratosis congenita with corneal limbal insufficiency.
Pediatric Blood & Cancer,
Vol. 53,
Issue. 1,
p.
95.