Results 141 to 150 of about 1,143,030 (232)

Immunoglobulin Light Chain Amyloidosis with Severe Liver Dysfunction Accompanied by Factor X Deficiency. [PDF]

Intern Med, 2019
Guo YM, Takahashi N, Miyabe K, Yoshida M, Abe F, Yamashita T, Nara M, Yoshioka T, Ohashi K, Goto A, Takahashi N.   +10 more
europepmc   +1 more source

Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: A critical evaluation [PDF]

, 2008
Antonio Girolami, Pamela Scarparo, Raffaella Scandellari, Emanuele Allemand   +3 more
openalex   +1 more source

Different genotypes are responsible for the normal Russell viper venom assays seen in some cases of congenital factor X deficiency [PDF]

, 2008
Antonio Girolami, Margherita Scapin, Pamela Scarparo, Silvia Vettore   +3 more
openalex   +1 more source

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients

British Journal of Haematology, 1998
F. Peyvandi, P. Mannucci, M. Lak, M. Abdoullahi, S. Zeinali, R. Sharifian, D. Perry   +6 more
semanticscholar   +1 more source

Factor X deficiency: an uncommon presentation of AL amyloidosis. [PDF]

Ups J Med Sci, 2012
Manikkan AT.
europepmc   +1 more source

Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency

, 2002
Frédéric Laumonnier, Nathalie Ronce, Ben C.J. Hamel, Paul Q. Thomas, James Lespinasse, Martine Raynaud, Christine Paringaux, Hans van Bokhoven, Vera M. Kalscheuer, Jean‐Pierre Fryns, Jamel Chelly, Claude Moraine, Sylvain Briault   +12 more
openalex   +1 more source

FACTOR X DEFICIENCY presenting as an intracranial bleed in a young infant

Sanyukta Sandeep Ghodke, Rishab Bhurat, Dhaarani Jayaraman, Sri Gayathri Shanmugam, Febe Renjitha Suman, Ramya Uppuluri, Rajakumar Padur Sivaraman, Julius Xavier Scott   +7 more
openalex   +1 more source

Tenascin-X deficiency causing classical-like Ehlers Danlos syndrome type 1 in humans is a significant risk factor for GI and tracheal ruptures.

Jonneke E. van Gurp, Rosan Lechner, Dimitra Micha, Alessandra Maugeri, Eelco Dulfer, Fleur S. van Dijk, Dániel Keszthelyi, Edoardo Malfatti, Akiharu Kubo, Nicol C. Voermans, Serwet Demirdas   +10 more
openalex   +1 more source

Congenital factor X deficiency: a case of unexplained neonatal anemia presenting with intracranial hemorrhage and hemorrhagic meningitis in the first month of life in a resource-limited setting

Radhapyari Lourembam, T. Arularasu, Amarjit Moirangthem, Shyamsunder Singh C.   +3 more
openalex   +1 more source

Membranoproliferative glomerulonephritis and a rare bleeding disorder: Factor X deficiency. [PDF]

Int Urol Nephrol, 2011
Basturk T, Ahbap E, Eroglu Kesim B, Yılmaz M, Koç Y, Sakacı T, Unsal A.   +6 more
europepmc   +1 more source