Results 71 to 80 of about 26,819 (157)

Severe polyarterial involvement in a 16-year-old with homozygous familial hypercholesterolaemia: a case report. [PDF]

Eur Heart J Case Rep
Benabdellah M, Mesfioui MB, El Ouartassi H, El Boussaadani B, Raissuni Z.   +4 more
europepmc   +1 more source

Two case reports of idiopathic prenatal closure of the ductus arteriosus complicated at birth by severe pulmonary hypertension successfully treated without intubation. [PDF]

Transl Pediatr
Mwizerwa L, Joye R, Cousin VL, Malaspinas I, Bouhabib M, Lucron H, Beghetti M, Wacker J.   +7 more
europepmc   +1 more source

Quelle place pour le travail ?

Revue Interventions Économiques, 2011
Olivier Cousin
doaj   +1 more source

Infantile-Onset Vanishing White Matter Disease in an Azerbaijani Infant With a Homozygous EIF2B5 p.(Arg195His) Variant. [PDF]

Cureus
Isayev C, Haciyeva I, Hasanov E, Hasanova F, Samadov P.   +4 more
europepmc   +1 more source

Amyloid Alpha: The Neglected Cousin of Amyloid Beta. [PDF]

Chembiochem
Raskatov JA.
europepmc   +1 more source

CCDC82 and neurodevelopment: a novel genetic variant linked to infantile spasms and hypotonia. [PDF]

BMC Med Genomics
Safarian Z, Mehrabi S, Rakhshani Nejad A, Alavimanesh S, Kavousinia P, Shushizadeh MH, Hassani SF, Onagh L, Sarli A, Rezaie N.   +9 more
europepmc   +1 more source

Early hypotonia and visual regression as presenting features of peroxisome biogenesis disorder: an Egyptian case report. [PDF]

BMC Pediatr
Sadek AA, Aladawy MA, Hassan K, Mansour TMM, Naser M, Elmoursy MM, Hedewy S, Hagag A, Mohamed KR, Abdelkreem E.   +9 more
europepmc   +1 more source

Home environment conditions during childhood and psychosocial outcomes across three generations in Sweden: population based adoption-discordant sibling comparison study.

BMJ
Liao Z, Zhou M, Brikell I, Chang Z, Kuja-Halkola R, D'Onofrio BM, Larsson H, Lichtenstein P, Pettersson E.   +8 more
europepmc   +1 more source

<i>DEGS1</i>-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of Literature. [PDF]

Neurol Genet
Grinberg M, Dale B, Ramachandrannair R, Tarnopolsky M, Whitney R, Ejaz R.   +5 more
europepmc   +1 more source