Results 121 to 130 of about 2,045 (160)

Age-dependent changes in infant head shape: a smartphone app-based study in Japan. [PDF]

Clin Pediatr Endocrinol
Narumi S, Honda Y, Kotoku Y, Eto H, Numasawa-Kuroiwa Y, Sakamoto Y, Kajita H, Miwa T, Nakahari A, Hosono S.   +9 more
europepmc   +1 more source

Sustained Erythroid Response to Eltrombopag in Low-Risk Myelodysplastic Neoplasms With Severe Anemia and Thrombocytopenia: A Case Report. [PDF]

Case Rep Hematol
Di Veroli A, De Gregoris C, Laureana R, Caridi M, Panichi V, Poscente M, Oliva EN, Latagliata R.   +7 more
europepmc   +1 more source

Very rare Palestinian case report of PRUNE1 p.Asp106Asn mutation: a mutation of global developmental delay. [PDF]

Ann Med Surg (Lond)
Idkaidak S, Abu-Hilal LH, Atawneh O, Janem AM, Alqarajeh F.   +4 more
europepmc   +1 more source

3-M syndrome: evolution of the phenotype over time. [PDF]

Ital J Pediatr
Bacchi I, Vandelli S, Coccia E, Giannini L, Zuntini R, Teneggi R, Caraffi SG, Baroni MC, Contrò G, Peruzzi A, Ambrosetti I, Pollazzon M, Sartori C, Lausch E, Matysiak U, Gambini L, Gargano G, Orlando V, Novelli A, Iughetti L, Unger S, Superti-Furga A, Garavelli L.   +22 more
europepmc   +1 more source

A rare case of split cord malformation type II with concomitant myelocystocele: illustrative case. [PDF]

J Neurosurg Case Lessons
Owen BS, Ivey NA, Bierbrauer KS, Nagaraj UD, Patel SK.   +4 more
europepmc   +1 more source

Perioperative insights into <i>KIF11</i> mutation-associated MLCRD syndrome in pediatric patients: First case report on anesthetic challenges. [PDF]

J Anaesthesiol Clin Pharmacol
Chauhan A, Ashwin M, Kumar A, Jha S.
europepmc   +1 more source

Beyond the Aorta: Incidental Atrial Septal Defect in a Patient With Marfan Syndrome and Severe Aortic Dilation. [PDF]

Cureus
Medina Santos FJ, Pérez Figueroa JE, Bonilla Figueroa RA, Acevedo Gómez KJ, Garro Almendaro AK, Cruz Villalobos RA, García Rodríguez JF.   +6 more
europepmc   +1 more source

A novel mutation of IFT140 in a preschool child with Mainzer-Saldino syndrome accompanied by rare tumor blastic plasmacytoid dendritic cell neoplasm: a case report. [PDF]

BMC Pediatr
Hu R, Li J, Yang F, Jiang M.
europepmc   +1 more source