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	21.	Hyperammonemia: A Silent Killer. [electronic resource] by Pallavi, Ranjita Matejak-Popis, Beata Producer: 20161222 In: American journal of therapeutics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Newborn screening and inborn errors of metabolism. [electronic resource] by Pasquali, Marzia Longo, Nicola Producer: 20110525 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 157C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Neurological manifestations of organic acidurias. [electronic resource] by Wajner, Moacir Producer: 20200124 In: Nature reviews. Neurology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	A rare cause of postpartum coma: isolated hyperammonemia due to urea cycle disorder. [electronic resource] by Açıkalın, Ayça Dişel, Nezihat Rana Producer: 20170406 In: The American journal of emergency medicine vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	An asymptomatic mother diagnosed with 3-methylcrotonyl-CoA carboxylase deficiency after newborn screening. [electronic resource] by Kör, Deniz Mungan, Neslihan Önenli Yılmaz, Berna Şeker Öktem, Murat Producer: 20160126 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	A commentary on short-term efficacy of N-carbamylglutamate in a patient with N-acetylglutamate synthase deficiency. [electronic resource] by Takayanagi, Masaki Producer: 20160120 In: Journal of human genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Late onset hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - how web searching by the family solved unexplained unconsciousness: a case report. [electronic resource] by Silfverberg, Thomas Sahlander, Fredrik Enlund, Magnus Oscarson, Mikael Hårdstedt, Maria Producer: 20190508 In: Journal of medical case reports vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Emergency Laboratory Evaluations for Patients With Inborn Errors of Metabolism. [electronic resource] by Gold, Nina B Kritzer, Amy Weiner, Debra L Michelson, Kenneth A Producer: 20211217 In: Pediatric emergency care vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Rare disease clinical research network's urea cycle consortium delivers a successful clinical trial to improve alternate pathway therapy. [electronic resource] by Mistry, Pramod K Producer: 20130816 In: Hepatology (Baltimore, Md.) vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	On the Creation, Utility and Sustaining of Rare Diseases Research Networks: Lessons learned from the Urea Cycle Disorders Consortium, the Japanese Urea Cycle Disorders Consortium and the European Registry and Network for Intoxication Type Metabolic Diseases. [electronic resource] by Summar, Marshall L Endo, Fumio Kölker, Stefan Producer: 20150610 In: Molecular genetics and metabolism vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Headache and neuropsychic disorders in the puerperium: a case report with suspected deficiency of urea cycle enzymes. [electronic resource] by Tonini, Maria Clara Bignamini, V Mattioli, M Producer: 20110817 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 32 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Urea cycle disorders-update. [electronic resource] by Matsumoto, Shirou Häberle, Johannes Kido, Jun Mitsubuchi, Hiroshi Endo, Fumio Nakamura, Kimitoshi Producer: 20191225 In: Journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Venovenous hemodiafiltration and hypothermia for treatment of cerebral edema associated with hyperammonemia. [electronic resource] by Vargha, R Möslinger, D Wagner, O Golej, J Producer: 20120914 In: Indian pediatrics vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	34.	Two Novel Heterozygous MCCC1 Mutations in a Neonate with Asymptomatic 3-methylcrotonyl-coenzyme A Carboxylase Deficiency. [electronic resource] by Yang, Bicheng Wang, Feng Producer: 20180926 In: Indian pediatrics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	35.	Nitrogen sparing therapy revisited 2009. [electronic resource] by Enns, Gregory M Producer: 20100721 In: Molecular genetics and metabolism vol. 100 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	The urea cycle disorders. [electronic resource] by Helman, Guy Pacheco-Colón, Ileana Gropman, Andrea L Producer: 20150602 In: Seminars in neurology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. [electronic resource] by Martinelli, Diego Diodato, Daria Ponzi, Emanuela Monné, Magnus Boenzi, Sara Bertini, Enrico Fiermonte, Giuseppe Dionisi-Vici, Carlo Producer: 20160121 In: Orphanet journal of rare diseases vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Encephalopathy mimicking non-convulsive status Epilepticus. [electronic resource] by Nandhagopal, Ramachandiran Al-Murshedi, Fathiya Al-Busaidi, Mujahid Al-Busaidi, Amna Producer: 20191016 In: Neurosciences (Riyadh, Saudi Arabia) vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Inborn Errors of Metabolism with Hyperammonemia: Urea Cycle Defects and Related Disorders. [electronic resource] by Summar, Marshall L Mew, Nicholas Ah Producer: 20181005 In: Pediatric clinics of North America vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Molecular modelling and dynamics of CA2 missense mutations causative to carbonic anhydrase 2 deficiency syndrome. [electronic resource] by Shaik, Noor A Bokhari, Hifaa A Masoodi, Tariq Ahmed Shetty, Preetha J Ajabnoor, Ghada M A Elango, Ramu Banaganapalli, Babajan Producer: 20210618 In: Journal of biomolecular structure & dynamics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 279 results.