Results 111 to 120 of about 31,187 (197)
[Aicardi-Goutières syndrome with atypical presentation: RNASEH2B gene mutation in an infant without microcephaly or intracranial calcifications (a case report)]. [PDF]
Iddir S +7 more
europepmc +1 more source
[Pulmonary hemosiderosis revealing class II HLA deficiency in a 9-month-old infant: a case report]. [PDF]
Beddi LH +6 more
europepmc +1 more source
[A case report of paraneoplastic Cushing's syndrome in young adults: a rare entity and real diagnostic challenge]. [PDF]
Sabbar G +4 more
europepmc +1 more source
[The timeline of the screening and treatment strategy of intraepithelial neoplasia of the uterine cervix adopted in Morocco]. [PDF]
Zraidi M, Ibriz M.
europepmc +1 more source

